{
 "dataset": "The Healthcare AI Transparency Registry",
 "source": "openFDA 510(k) records under AI-associated product codes",
 "publisher": "The Healthcare AI Institute — healthcareaiops.com/registry/",
 "license": "CC BY 4.0",
 "count": 558,
 "entries": [
  {
   "k_number": "K262452",
   "device_name": "AutoContour (RADAC V6)",
   "applicant": "Radformation, Inc.",
   "decision_date": "2026-08-14",
   "product_code": "QKB",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K260898",
   "device_name": "Transpara (2.1.0)",
   "applicant": "Screenpoint Medical B.V.",
   "decision_date": "2026-08-14",
   "product_code": "QDQ",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "NL"
  },
  {
   "k_number": "K260086",
   "device_name": "CadAI-B Dx",
   "applicant": "BeamWorks, Inc.",
   "decision_date": "2026-08-12",
   "product_code": "QDQ",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K253794",
   "device_name": "Prostate Core",
   "applicant": "Lucida Medical, Ltd.",
   "decision_date": "2026-08-10",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "GB"
  },
  {
   "k_number": "K252571",
   "device_name": "mdprostate",
   "applicant": "Mediaire GmbH",
   "decision_date": "2026-08-07",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "DE"
  },
  {
   "k_number": "K253902",
   "device_name": "RealGUIDE",
   "applicant": "3DIEMME SRL",
   "decision_date": "2026-08-04",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IT"
  },
  {
   "k_number": "K253835",
   "device_name": "Affinity",
   "applicant": "Hermes Medical Solutions AB",
   "decision_date": "2026-07-31",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "SE"
  },
  {
   "k_number": "K260980",
   "device_name": "cmAngio® V2.0",
   "applicant": "Curemetrix, Inc.",
   "decision_date": "2026-07-30",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K261210",
   "device_name": "Cleerly Plaque",
   "applicant": "Cleerly, Inc.",
   "decision_date": "2026-07-29",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K260303",
   "device_name": "See-Mode Augmented Reporting Tool, Breast (SMART-B)",
   "applicant": "See-Mode Technologies Pty, Ltd.",
   "decision_date": "2026-07-28",
   "product_code": "QDQ",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "AU"
  },
  {
   "k_number": "K260192",
   "device_name": "DIANA",
   "applicant": "ROPCA ApS",
   "decision_date": "2026-07-24",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "DK"
  },
  {
   "k_number": "K261349",
   "device_name": "SwiftMR",
   "applicant": "Airs Medical, Inc.",
   "decision_date": "2026-07-24",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K254096",
   "device_name": "VELMENI for DENTISTS (V4D) 3D",
   "applicant": "Velmeni, Inc.",
   "decision_date": "2026-07-23",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K261535",
   "device_name": "Hi-D Imaging 4TAVR",
   "applicant": "Hi-D Imaging AG",
   "decision_date": "2026-07-20",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CH"
  },
  {
   "k_number": "K260338",
   "device_name": "ThinkSono Guidance",
   "applicant": "ThinkSono GmbH",
   "decision_date": "2026-07-15",
   "product_code": "QJU",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "DE"
  },
  {
   "k_number": "K260206",
   "device_name": "SkeletonPlanner",
   "applicant": "UPlanner B.V. - Presurgeo",
   "decision_date": "2026-07-15",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "NL"
  },
  {
   "k_number": "K261085",
   "device_name": "Rapid Vessel Occlusion (Rapid VO)",
   "applicant": "iSchemaview",
   "decision_date": "2026-07-13",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K261306",
   "device_name": "AI Contouring (VA10A)",
   "applicant": "Varian Medical Systems",
   "decision_date": "2026-07-10",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K253751",
   "device_name": "CXRDetectAI",
   "applicant": "Neurocareai, Inc. (Dba Savelife.Ai)",
   "decision_date": "2026-07-08",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K260973",
   "device_name": "InferOperate Suite",
   "applicant": "Beijing Infervision Healthcare Medical Technology Co., Ltd.",
   "decision_date": "2026-07-07",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CN"
  },
  {
   "k_number": "K260528",
   "device_name": "OncoStudio",
   "applicant": "Oncosoft. Inc.,",
   "decision_date": "2026-07-02",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K253969",
   "device_name": "ADAS 3D",
   "applicant": "Adas3D Medical S.L.",
   "decision_date": "2026-06-29",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "ES"
  },
  {
   "k_number": "K253628",
   "device_name": "Auto-Seg (SO-0012), Spine Auto-Seg (SO-0012)",
   "applicant": "Agada Medical, Ltd.",
   "decision_date": "2026-06-29",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K260714",
   "device_name": "MammoScreen® (5)",
   "applicant": "Therapixel",
   "decision_date": "2026-06-26",
   "product_code": "QDQ",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K253786",
   "device_name": "syngo.CT Coronary Cockpit",
   "applicant": "Siemens Medical Solutions USA, Inc.",
   "decision_date": "2026-06-25",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K260316",
   "device_name": "CMN Capillary Function with Oncology Virtual Expert",
   "applicant": "Cercare Medical A/S",
   "decision_date": "2026-06-22",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "DK"
  },
  {
   "k_number": "K261713",
   "device_name": "Synapse PACS (7.6.0)",
   "applicant": "FUJIFILM Healthcare Americas Corporation",
   "decision_date": "2026-06-18",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K260729",
   "device_name": "Vascular Assist Occlusion Triage (VAOT) (v1.0)",
   "applicant": "GuideAI Health",
   "decision_date": "2026-06-18",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K253172",
   "device_name": "MediAI-OA",
   "applicant": "Crescom Co., Ltd.",
   "decision_date": "2026-06-15",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K260300",
   "device_name": "WatchMate Software",
   "applicant": "Anumana, Inc.",
   "decision_date": "2026-06-15",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K253690",
   "device_name": "LungMaps",
   "applicant": "Siemens Healthineers AG",
   "decision_date": "2026-06-15",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "DE"
  },
  {
   "k_number": "K253825",
   "device_name": "Saige-Dx",
   "applicant": "DeepHealth, Inc.",
   "decision_date": "2026-06-15",
   "product_code": "QDQ",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K260406",
   "device_name": "Brainomix 360 Hyperdensity",
   "applicant": "Brainomix Limited",
   "decision_date": "2026-06-12",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "GB"
  },
  {
   "k_number": "K260322",
   "device_name": "Acorn 3D Software (AC-SEG-4009); Acorn 3DP Model (AC-101-XX)",
   "applicant": "Mighty Oak Medical",
   "decision_date": "2026-06-11",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K260497",
   "device_name": "DEEPVESSEL Plaque",
   "applicant": "Keya Medical Technology Co., Ltd.",
   "decision_date": "2026-06-04",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CN"
  },
  {
   "k_number": "K260780",
   "device_name": "HeartFocus",
   "applicant": "Deski",
   "decision_date": "2026-06-03",
   "product_code": "QJU",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K260077",
   "device_name": "OrthoGrid Hip AI® 4.0",
   "applicant": "OrthoGrid Systems, Inc.",
   "decision_date": "2026-05-29",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K261405",
   "device_name": "ANDI 2.2",
   "applicant": "Imeka Solutions, Inc.",
   "decision_date": "2026-05-28",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CA"
  },
  {
   "k_number": "K260324",
   "device_name": "Vitrea CT Transcatheter Aortic Valve Replacement (TAVR) Planning",
   "applicant": "Canon Medical Informatics, Inc.",
   "decision_date": "2026-05-22",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K254131",
   "device_name": "BAC",
   "applicant": "DeepHealth, Inc.",
   "decision_date": "2026-05-21",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K260234",
   "device_name": "MSK Go",
   "applicant": "Smart Alfa Teknoloji San. Ve Tic. A.S.",
   "decision_date": "2026-05-21",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "TR"
  },
  {
   "k_number": "K254120",
   "device_name": "SubtleHD-CT (1.x)",
   "applicant": "Subtle Medical, Inc.",
   "decision_date": "2026-05-15",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K261289",
   "device_name": "UNiD™ Spine Analyzer (SW3002)",
   "applicant": "Medicrea International S.A.S. (Medtronic)",
   "decision_date": "2026-05-15",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K261273",
   "device_name": "Neurophet AQUA",
   "applicant": "Neurophet., Inc.",
   "decision_date": "2026-05-15",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K252563",
   "device_name": "Neurophet SCALE PET",
   "applicant": "Neurophet., Inc.",
   "decision_date": "2026-05-15",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K261317",
   "device_name": "BriefCase-Triage",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2026-05-14",
   "product_code": "QAS",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K260032",
   "device_name": "Morph",
   "applicant": "BeauBrain Healthcare, Inc.",
   "decision_date": "2026-05-13",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K260378",
   "device_name": "Rayvolve",
   "applicant": "AZmed",
   "decision_date": "2026-05-12",
   "product_code": "QBS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K252954",
   "device_name": "MammoSightAI",
   "applicant": "Neurocareai, Inc. (Dba Savelife.Ai)",
   "decision_date": "2026-05-04",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K254189",
   "device_name": "Synapse 3D Base Tools (V7.2)",
   "applicant": "Fujifilm Corporation",
   "decision_date": "2026-04-30",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "JP"
  },
  {
   "k_number": "K254184",
   "device_name": "syngo Application Software",
   "applicant": "Siemens Medical Solutions USA, Inc.",
   "decision_date": "2026-04-29",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K253682",
   "device_name": "DeepHealth ProstateAI",
   "applicant": "Quantib B.V.",
   "decision_date": "2026-04-29",
   "product_code": "QDQ",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "NL"
  },
  {
   "k_number": "K260785",
   "device_name": "DS Core CBCT Anatomy",
   "applicant": "Dentsply Sirona",
   "decision_date": "2026-04-23",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K260320",
   "device_name": "Lunit INSIGHT MMG (v1.1.10)",
   "applicant": "Lunit, Inc.",
   "decision_date": "2026-04-23",
   "product_code": "QDQ",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K253077",
   "device_name": "uOmnispace.MR",
   "applicant": "Shanghai United Imaging Healthcare Co., Ltd.",
   "decision_date": "2026-04-22",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CN"
  },
  {
   "k_number": "K253163",
   "device_name": "EFAI ERSUITE CT APPENDICITIS ASSESSMENT SYSTEM (APPEN-CT-100)",
   "applicant": "Ever Fortune.Ai, Co., Ltd.",
   "decision_date": "2026-04-22",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "TW"
  },
  {
   "k_number": "K252332",
   "device_name": "Folliscan",
   "applicant": "Mim Fertility",
   "decision_date": "2026-04-20",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "PL"
  },
  {
   "k_number": "K253502",
   "device_name": "Critical Care Suite with Enteric Tube Positioning AI Algorithm",
   "applicant": "Ge Medical Systems, LLC",
   "decision_date": "2026-04-14",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K252548",
   "device_name": "AI-Rad Companion Organs RT",
   "applicant": "Siemens Healthcare GmbH",
   "decision_date": "2026-04-10",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "DE"
  },
  {
   "k_number": "K252190",
   "device_name": "DeepBT Detector-Plus",
   "applicant": "Aitewan Biomedical Technology, Inc.",
   "decision_date": "2026-04-10",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "TW"
  },
  {
   "k_number": "K253689",
   "device_name": "syngo Dynamics (VA41F)",
   "applicant": "Siemens Healthcare GmbH",
   "decision_date": "2026-04-10",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "DE"
  },
  {
   "k_number": "K252708",
   "device_name": "Relu Cloud",
   "applicant": "Relu BV",
   "decision_date": "2026-04-10",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "BE"
  },
  {
   "k_number": "K253930",
   "device_name": "Overjet Iris Intelligent Imaging System",
   "applicant": "Overjet, Inc.",
   "decision_date": "2026-04-10",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K254015",
   "device_name": "CoLumbo C-Spine",
   "applicant": "Smart Soft Healthcare AD",
   "decision_date": "2026-04-01",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "BG"
  },
  {
   "k_number": "K254207",
   "device_name": "AiORTA - Plan v2.0",
   "applicant": "ViTAA Medical Solutions, Inc.",
   "decision_date": "2026-03-30",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CA"
  },
  {
   "k_number": "K253270",
   "device_name": "Contour ProtégéAI+",
   "applicant": "Mim Software, Inc.",
   "decision_date": "2026-03-27",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K253775",
   "device_name": "SwiftMR",
   "applicant": "Airs Medical, Inc.",
   "decision_date": "2026-03-26",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K253796",
   "device_name": "Lunit INSIGHT DBT (V1.2)",
   "applicant": "Lunit, Inc.",
   "decision_date": "2026-03-26",
   "product_code": "QDQ",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K252421",
   "device_name": "JLK-NCCT",
   "applicant": "JLK, Inc.",
   "decision_date": "2026-03-24",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K260509",
   "device_name": "AutoContour (RADAC V5)",
   "applicant": "Radformation, Inc.",
   "decision_date": "2026-03-19",
   "product_code": "QKB",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K253614",
   "device_name": "EchoNavigator R5.0",
   "applicant": "Philips Medical Systems Nederland B.V.",
   "decision_date": "2026-03-17",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "NL"
  },
  {
   "k_number": "K253944",
   "device_name": "Data Analysis Facilitation Suite (DAFS)",
   "applicant": "Voronoi Health Analytics Incorporated",
   "decision_date": "2026-03-16",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CA"
  },
  {
   "k_number": "K252261",
   "device_name": "InferCare RECIST",
   "applicant": "Beijing Infervision Healthcare Medical Technology Co., Ltd.",
   "decision_date": "2026-03-13",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CN"
  },
  {
   "k_number": "K253551",
   "device_name": "VELYS™ Hip Navigation",
   "applicant": "Depuy Ireland UC",
   "decision_date": "2026-03-06",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IE"
  },
  {
   "k_number": "K252538",
   "device_name": "CEPHX3D",
   "applicant": "Orca Dental AI , Ltd.",
   "decision_date": "2026-03-05",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K253818",
   "device_name": "Annalise Enterprise",
   "applicant": "Harrison-AI Medical Pty, Ltd.",
   "decision_date": "2026-03-03",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "AU"
  },
  {
   "k_number": "K253593",
   "device_name": "Clarius Ejection Fraction AI",
   "applicant": "Clarius Mobile Health Corp.",
   "decision_date": "2026-03-02",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CA"
  },
  {
   "k_number": "K253535",
   "device_name": "Ligence Heart",
   "applicant": "Ligence Uab",
   "decision_date": "2026-02-27",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "LT"
  },
  {
   "k_number": "K253578",
   "device_name": "BriefCase-Triage: CARE Multi-Triage CT for Pneumothorax; Pericardial effusion; Large aortic aneurysm; Shoulder fracture or dislocation device",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2026-02-26",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K260217",
   "device_name": "AI Platform 2.2 (AIP002)",
   "applicant": "Exo Imaging",
   "decision_date": "2026-02-24",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K252084",
   "device_name": "AI4CMR v2.0",
   "applicant": "Ai4medimaging Medical Solutions S.A.",
   "decision_date": "2026-02-11",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "PT"
  },
  {
   "k_number": "K254016",
   "device_name": "MI View&GO",
   "applicant": "Siemens Medical Solutions USA, Inc.",
   "decision_date": "2026-02-10",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K251474",
   "device_name": "Median LCS (internal name) / eyonis LCS (trade name) (1.0)",
   "applicant": "Median Technologies",
   "decision_date": "2026-02-06",
   "product_code": "QDQ",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K252091",
   "device_name": "Surgical Reality Viewer",
   "applicant": "Medicalvr B.V.",
   "decision_date": "2026-01-29",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "NL"
  },
  {
   "k_number": "K252496",
   "device_name": "Neurophet AQUA AD Plus",
   "applicant": "Neurophet., Inc.",
   "decision_date": "2026-01-29",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K251306",
   "device_name": "Seg Pro V3 (RT-300)",
   "applicant": "Ever Fortune.Ai, Co., Ltd.",
   "decision_date": "2026-01-28",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "TW"
  },
  {
   "k_number": "K251195",
   "device_name": "BriefCase-Triage",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2026-01-27",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K251351",
   "device_name": "AccuContour 4.0",
   "applicant": "Manteia Technologies Co., Ltd.",
   "decision_date": "2026-01-23",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CN"
  },
  {
   "k_number": "K253057",
   "device_name": "AI-Rad Companion Brain MR",
   "applicant": "Siemens Healthcare GmbH",
   "decision_date": "2026-01-22",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "DE"
  },
  {
   "k_number": "K253735",
   "device_name": "AV Vascular",
   "applicant": "Philips Medical Systems Nederland B.V.",
   "decision_date": "2026-01-22",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "NL"
  },
  {
   "k_number": "K252634",
   "device_name": "Imagine® Enterprise Suite",
   "applicant": "Softlink International Private Limited",
   "decision_date": "2026-01-16",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IN"
  },
  {
   "k_number": "K252970",
   "device_name": "BriefCase-Triage: CARE Multi-triage CT Body",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2026-01-07",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K253532",
   "device_name": "TruSPECT Processing Station",
   "applicant": "Spectrum Dynamics Medical, Ltd.",
   "decision_date": "2025-12-30",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K252856",
   "device_name": "PeekMed web",
   "applicant": "Peek Health, S.A.",
   "decision_date": "2025-12-22",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "PT"
  },
  {
   "k_number": "K252029",
   "device_name": "AI-CVD",
   "applicant": "HeartLung Corporation",
   "decision_date": "2025-12-19",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K252670",
   "device_name": "Alzevita",
   "applicant": "TOPIA MEDTECH LIMITED",
   "decision_date": "2025-12-19",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "GB"
  },
  {
   "k_number": "K250914",
   "device_name": "MediAI-BA",
   "applicant": "Crescom Co., Ltd.",
   "decision_date": "2025-12-18",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K252235",
   "device_name": "PVAD IQ Software",
   "applicant": "Ultrasight , Ltd.",
   "decision_date": "2025-12-18",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K251416",
   "device_name": "UltraSight Guidance",
   "applicant": "Ultrasight , Ltd.",
   "decision_date": "2025-12-17",
   "product_code": "QJU",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K252922",
   "device_name": "Neosoma Brain Mets",
   "applicant": "Neosoma, Inc.",
   "decision_date": "2025-12-17",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K251763",
   "device_name": "IRISeg",
   "applicant": "Intuitive Surgical, Inc.",
   "decision_date": "2025-12-16",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K252482",
   "device_name": "CogNet AI-MT+",
   "applicant": "Medcognetics, Inc.",
   "decision_date": "2025-12-11",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K250780",
   "device_name": "ARTAssistant",
   "applicant": "Manteia Technologies Co., Ltd.",
   "decision_date": "2025-12-05",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CN"
  },
  {
   "k_number": "K251514",
   "device_name": "Overjet CBCT Assist",
   "applicant": "Overjet, Inc.",
   "decision_date": "2025-12-05",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K252103",
   "device_name": "Acorn 3D Software (AC-SEG-4009); Acorn 3DP Model (AC-101-XX)",
   "applicant": "Mighty Oak Medical",
   "decision_date": "2025-12-02",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K250694",
   "device_name": "Scaida BrainCT-ICH (v1.0)",
   "applicant": "Mlhealth 360",
   "decision_date": "2025-11-25",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CA"
  },
  {
   "k_number": "K252366",
   "device_name": "a2z-Unified-Triage",
   "applicant": "A2z Radiology Ai, Inc.",
   "decision_date": "2025-11-24",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K251078",
   "device_name": "AutoDensity",
   "applicant": "Eos Imaging",
   "decision_date": "2025-11-14",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K252452",
   "device_name": "PeekMed web",
   "applicant": "Peek Health, S.A.",
   "decision_date": "2025-11-12",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "PT"
  },
  {
   "k_number": "K253265",
   "device_name": "BriefCase-Triage",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2025-11-06",
   "product_code": "QAS",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K250330",
   "device_name": "3mensio Workstation",
   "applicant": "Pie Medical Imaging BV",
   "decision_date": "2025-11-03",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "NL"
  },
  {
   "k_number": "K250337",
   "device_name": "AiORTA - Plan",
   "applicant": "ViTAA Medical Solutions, Inc.",
   "decision_date": "2025-10-30",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CA"
  },
  {
   "k_number": "K251027",
   "device_name": "cvi42 Coronary Plaque Software Application",
   "applicant": "Circle Cardiovascular Imaging, Inc.",
   "decision_date": "2025-10-27",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CA"
  },
  {
   "k_number": "K251059",
   "device_name": "Syngo Carbon Clinicals (VA41)",
   "applicant": "Siemens Healthineers AG",
   "decision_date": "2025-10-24",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "DE"
  },
  {
   "k_number": "K250288",
   "device_name": "TeraRecon Cardiovascular.Calcification.CT",
   "applicant": "Terarecon,Inc.",
   "decision_date": "2025-10-23",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K252298",
   "device_name": "ANDI 2.0",
   "applicant": "Imeka Solutions, Inc.",
   "decision_date": "2025-10-22",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CA"
  },
  {
   "k_number": "K252665",
   "device_name": "brAIn™ Shoulder Positioning",
   "applicant": "Avatar Medical",
   "decision_date": "2025-10-20",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K252214",
   "device_name": "AIAS Cephalon",
   "applicant": "Metamorphosis GmbH",
   "decision_date": "2025-10-07",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "DE"
  },
  {
   "k_number": "K252007",
   "device_name": "BlineSlide",
   "applicant": "Deep Breathe, Inc.",
   "decision_date": "2025-10-06",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CA"
  },
  {
   "k_number": "K250023",
   "device_name": "SMART PCFD",
   "applicant": "Disior, Ltd.",
   "decision_date": "2025-09-29",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FI"
  },
  {
   "k_number": "K252105",
   "device_name": "Ligence Heart",
   "applicant": "Ligence Uab",
   "decision_date": "2025-09-26",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "LT"
  },
  {
   "k_number": "K251527",
   "device_name": "Brain WMH",
   "applicant": "Quantib B.V.",
   "decision_date": "2025-09-25",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "NL"
  },
  {
   "k_number": "K251483",
   "device_name": "SwiftSight-Brain",
   "applicant": "Airs Medical, Inc.",
   "decision_date": "2025-09-23",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K251987",
   "device_name": "Rapid Aortic Measurements",
   "applicant": "Ischemaview, Inc.",
   "decision_date": "2025-09-23",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K250369",
   "device_name": "Axial3D Insight",
   "applicant": "Axial Medical Printing Limited",
   "decision_date": "2025-09-18",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "GB"
  },
  {
   "k_number": "K250237",
   "device_name": "InferOperate Suite",
   "applicant": "Beijing Infervision Healthcare Medical Technology Co., Ltd.",
   "decision_date": "2025-09-15",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CN"
  },
  {
   "k_number": "K244002",
   "device_name": "AngioWaveNet",
   "applicant": "Angiowave Imaging, Inc.",
   "decision_date": "2025-09-10",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K251072",
   "device_name": "Segmentron Viewer",
   "applicant": "DGNCT, LLC",
   "decision_date": "2025-09-09",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K251610",
   "device_name": "qER-CTA (v1.0)",
   "applicant": "Qure.Ai Technologies",
   "decision_date": "2025-09-08",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IN"
  },
  {
   "k_number": "K251656",
   "device_name": "Careverse CoronaryDoc (Careverse CoronaryDoc)",
   "applicant": "Careverse Technology Pte. , Ltd.",
   "decision_date": "2025-09-04",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "SG"
  },
  {
   "k_number": "K251533",
   "device_name": "Rapid Obstructive Hydrocephalus, Rapid OH",
   "applicant": "Ischemaview, Inc.",
   "decision_date": "2025-09-04",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K252539",
   "device_name": "Tempus Pixel",
   "applicant": "Arterys, Inc.",
   "decision_date": "2025-09-03",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K243859",
   "device_name": "PRAEVAorta®2",
   "applicant": "Nurea",
   "decision_date": "2025-08-29",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K250947",
   "device_name": "VistaSoft 4.0 and VisionX 4.0",
   "applicant": "Durr Dental SE",
   "decision_date": "2025-08-27",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "DE"
  },
  {
   "k_number": "K251983",
   "device_name": "Brainomix 360 Triage Stroke",
   "applicant": "Brainomix Limited",
   "decision_date": "2025-08-26",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "GB"
  },
  {
   "k_number": "K252362",
   "device_name": "GBrain MRI",
   "applicant": "Galileo Cds, Inc.",
   "decision_date": "2025-08-22",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K243685",
   "device_name": "MammoScreen BD",
   "applicant": "Therapixel",
   "decision_date": "2025-08-22",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K251837",
   "device_name": "Salix Coronary Plaque (V1.0.0)",
   "applicant": "Artrya Limited",
   "decision_date": "2025-08-20",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "AU"
  },
  {
   "k_number": "K251590",
   "device_name": "Methinks CTA Stroke",
   "applicant": "Methinks Software, S.L",
   "decision_date": "2025-08-20",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "ES"
  },
  {
   "k_number": "K251747",
   "device_name": "VEA Align; spineEOS",
   "applicant": "Eos Imaging",
   "decision_date": "2025-08-15",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K250755",
   "device_name": "DS Core Diagnosis",
   "applicant": "Dentsply Sirona, Inc.",
   "decision_date": "2025-08-12",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K251873",
   "device_name": "Saige-Dx",
   "applicant": "DeepHealth, Inc.",
   "decision_date": "2025-08-11",
   "product_code": "QDQ",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K251629",
   "device_name": "UNiD™ Spine Analyzer",
   "applicant": "Medicrea International S.A.S. (Medtronic)",
   "decision_date": "2025-08-07",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K243341",
   "device_name": "Genius AI Detection 2.0",
   "applicant": "Hologic, Inc.",
   "decision_date": "2025-07-31",
   "product_code": "QDQ",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K243919",
   "device_name": "Voxel Dosimetry (00859873006226)",
   "applicant": "Hermes Medical Solutions AB",
   "decision_date": "2025-07-30",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "SE"
  },
  {
   "k_number": "K251342",
   "device_name": "EchoPAC Software Only / EchoPAC Plug-in",
   "applicant": "GE Medical Systems Ultrasound and Primary Care Diagnostics",
   "decision_date": "2025-07-16",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K251151",
   "device_name": "Rapid CTA 360",
   "applicant": "Ischemaview",
   "decision_date": "2025-07-16",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K251096",
   "device_name": "PeekMed web",
   "applicant": "Peek Health, S.A.",
   "decision_date": "2025-07-14",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "PT"
  },
  {
   "k_number": "K251766",
   "device_name": "TumorSight Viz",
   "applicant": "SimBioSys, Inc.",
   "decision_date": "2025-07-08",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K251528",
   "device_name": "syngo.via MI Workflows; Scenium; syngo MBF",
   "applicant": "Siemens Medical Solutions USA, Inc.",
   "decision_date": "2025-07-03",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K243679",
   "device_name": "MammoScreen® (4)",
   "applicant": "Therapixel",
   "decision_date": "2025-07-03",
   "product_code": "QDQ",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K243779",
   "device_name": "Bunkerhill Abdominal Aortic Quantification (AAQ)",
   "applicant": "BunkerHill Health",
   "decision_date": "2025-07-01",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K243647",
   "device_name": "Synapse PACS (7.5)",
   "applicant": "FUJIFILM Healthcare Americas Corporation",
   "decision_date": "2025-06-30",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K250670",
   "device_name": "EchoConfidence (USA)",
   "applicant": "Mycardium AI Limited",
   "decision_date": "2025-06-30",
   "product_code": "QIH",
   "clearance_type": "Abbreviated",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "GB"
  },
  {
   "k_number": "K250484",
   "device_name": "PIUR tUS inside",
   "applicant": "Piur Imaging GmbH",
   "decision_date": "2025-06-30",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "AT"
  },
  {
   "k_number": "K250685",
   "device_name": "Methinks NCCT Stroke",
   "applicant": "Methinks Software, S.L",
   "decision_date": "2025-06-16",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "ES"
  },
  {
   "k_number": "K243633",
   "device_name": "Brainlab Elements (7.0); Brainlab Elements Image Fusion (5.0); Brainlab Elements Image Fusion Angio (1.0); Brainlab Elements Contouring (5.0); Brainlab Elements Fibertracking (3.0); Brainlab Elements ",
   "applicant": "Brainlab AG",
   "decision_date": "2025-06-13",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "DE"
  },
  {
   "k_number": "K250354",
   "device_name": "Viz Subdural+, Viz SUBDURAL PLUS",
   "applicant": "Viz. Ai, Inc.",
   "decision_date": "2025-06-10",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K251009",
   "device_name": "Cirrus Resting State fMRI Software",
   "applicant": "Sora Neuroscience, Inc.",
   "decision_date": "2025-06-06",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K251456",
   "device_name": "BrightHeart View Classifier",
   "applicant": "Brightheart",
   "decision_date": "2025-06-05",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K243810",
   "device_name": "TraumaCad Neo (1.1)",
   "applicant": "Brainlab , Ltd.",
   "decision_date": "2025-06-04",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K243863",
   "device_name": "Opulus™ Lymphoma Precision",
   "applicant": "Roche Molecular Systems, Inc.",
   "decision_date": "2025-05-30",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K243005",
   "device_name": "AudaxCeph Cephalogram Analysis Software",
   "applicant": "Audax D.O.O.",
   "decision_date": "2025-05-30",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "SI"
  },
  {
   "k_number": "K251406",
   "device_name": "BriefCase-Triage",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2025-05-30",
   "product_code": "QAS",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K250427",
   "device_name": "TAIMedImg DeepMets",
   "applicant": "Taiwan Medical Imaging Co., Ltd.",
   "decision_date": "2025-05-28",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "TW"
  },
  {
   "k_number": "K250367",
   "device_name": "CoLumboX",
   "applicant": "Smart Soft Healthcare AD",
   "decision_date": "2025-05-28",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "BG"
  },
  {
   "k_number": "K243378",
   "device_name": "Rapid MLS",
   "applicant": "Ischemaview, Inc.",
   "decision_date": "2025-05-28",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K250005",
   "device_name": "Clever One",
   "applicant": "Ewoosoft Co., Ltd.",
   "decision_date": "2025-05-23",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K243989",
   "device_name": "Second Opinion® 3D",
   "applicant": "Pearl, Inc.",
   "decision_date": "2025-05-23",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K243762",
   "device_name": "Synapse 3D Base Tools (V7.0)",
   "applicant": "Fujifilm Corporation",
   "decision_date": "2025-05-21",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "JP"
  },
  {
   "k_number": "K242624",
   "device_name": "Medical Image Post-processing Software (uOmnispace.CT)",
   "applicant": "Shanghai United Imaging Healthcare Co., Ltd.",
   "decision_date": "2025-05-14",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CN"
  },
  {
   "k_number": "K243230",
   "device_name": "Second Opinion® BLE",
   "applicant": "Pearl, Inc.",
   "decision_date": "2025-05-09",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K250226",
   "device_name": "Clarius Median Nerve AI",
   "applicant": "Clarius Mobile Health Corp.",
   "decision_date": "2025-05-08",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CA"
  },
  {
   "k_number": "K243684",
   "device_name": "BrightHeart View Classifier",
   "applicant": "Brightheart",
   "decision_date": "2025-05-07",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K250328",
   "device_name": "UltraExtend NX CUW-U001S V2.0 Ultrasound Image Analysis Program",
   "applicant": "Canon Medical Systems Corporation",
   "decision_date": "2025-04-30",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "JP"
  },
  {
   "k_number": "K250831",
   "device_name": "Annalise Enterprise",
   "applicant": "Annalise-Ai",
   "decision_date": "2025-04-23",
   "product_code": "QFM",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "AU"
  },
  {
   "k_number": "K242500",
   "device_name": "LARALAB",
   "applicant": "Laralab GmbH",
   "decision_date": "2025-04-16",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "DE"
  },
  {
   "k_number": "K243853",
   "device_name": "Clarius Prostate AI",
   "applicant": "Clarius Mobile Health Corp.",
   "decision_date": "2025-04-16",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CA"
  },
  {
   "k_number": "K250416",
   "device_name": "GBrain MRI",
   "applicant": "Galileo Cds, Inc.",
   "decision_date": "2025-04-11",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K250754",
   "device_name": "cmAngio® (V1.6)",
   "applicant": "Curemetrix, Inc.",
   "decision_date": "2025-04-10",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K243145",
   "device_name": "syngo.CT LVO Detection",
   "applicant": "Siemens Medical Solutions USA, Inc.",
   "decision_date": "2025-04-10",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K242807",
   "device_name": "HeartFocus (V.1.1.1)",
   "applicant": "Deski",
   "decision_date": "2025-04-04",
   "product_code": "QJU",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K241982",
   "device_name": "DeepFoqus (DeepFoqus-Accelerate)",
   "applicant": "Foqus Technologies, Inc.",
   "decision_date": "2025-04-04",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CA"
  },
  {
   "k_number": "K242551",
   "device_name": "syngo Dynamics (Version VA41D)",
   "applicant": "Siemens Healthcare GmbH",
   "decision_date": "2025-04-03",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "DE"
  },
  {
   "k_number": "K241984",
   "device_name": "Hi-D Imaging 4TAVR",
   "applicant": "Hi-D Imaging AG",
   "decision_date": "2025-04-02",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CH"
  },
  {
   "k_number": "K242925",
   "device_name": "MR Contour DL",
   "applicant": "GE Healthcare",
   "decision_date": "2025-04-01",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K242166",
   "device_name": "TribusConnect",
   "applicant": "Tribusmed Beheer BV",
   "decision_date": "2025-03-31",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "NL"
  },
  {
   "k_number": "K242745",
   "device_name": "AI-Rad Companion Organs RT",
   "applicant": "Siemens Healthcare GmbH",
   "decision_date": "2025-03-27",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "DE"
  },
  {
   "k_number": "K243038",
   "device_name": "Salix Central",
   "applicant": "Artrya Limited",
   "decision_date": "2025-03-27",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "AU"
  },
  {
   "k_number": "K243808",
   "device_name": "Rayvolve PTX-PE",
   "applicant": "AZmed",
   "decision_date": "2025-03-21",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K241961",
   "device_name": "Vent Creativity Knee v1.0 (Hermes)",
   "applicant": "Vent Creativity",
   "decision_date": "2025-03-20",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K243689",
   "device_name": "AVIEW",
   "applicant": "Coreline Soft Co., Ltd.",
   "decision_date": "2025-03-19",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K250042",
   "device_name": "PeekMed web",
   "applicant": "Peek Health, S.A.",
   "decision_date": "2025-03-19",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "PT"
  },
  {
   "k_number": "K242683",
   "device_name": "QP-Prostate® CAD",
   "applicant": "Quibim S.L.",
   "decision_date": "2025-03-18",
   "product_code": "QDQ",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "ES"
  },
  {
   "k_number": "K243862",
   "device_name": "LVivo Software Application",
   "applicant": "Dia Imaging Analysis, Ltd.",
   "decision_date": "2025-03-17",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K242338",
   "device_name": "Cleerly LABS (v2.0)",
   "applicant": "Cleerly, Inc.",
   "decision_date": "2025-03-07",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K243331",
   "device_name": "LVivo Seamless",
   "applicant": "Dia Imaging Analysis, Ltd.",
   "decision_date": "2025-03-06",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K241770",
   "device_name": "Prostate MR AI (VA10A)",
   "applicant": "Siemens Healthcare GmbH",
   "decision_date": "2025-03-05",
   "product_code": "QDQ",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "DE"
  },
  {
   "k_number": "K243933",
   "device_name": "Ceevra Reveal 3+",
   "applicant": "Ceevra, Inc.",
   "decision_date": "2025-03-04",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K243235",
   "device_name": "LVivo Software Application",
   "applicant": "Dia Imaging Analysis, Ltd.",
   "decision_date": "2025-03-03",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K243611",
   "device_name": "JLK-SDH",
   "applicant": "JLK, Inc.",
   "decision_date": "2025-03-03",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K241922",
   "device_name": "Myomics",
   "applicant": "Phantomics, Inc.",
   "decision_date": "2025-02-28",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K241222",
   "device_name": "Ventripoint Medical System Plus (VMS+) 4.0",
   "applicant": "Ventripoint Diagnostics , Ltd.",
   "decision_date": "2025-02-26",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CA"
  },
  {
   "k_number": "K242994",
   "device_name": "OncoStudio (OS-01)",
   "applicant": "Oncosoft. Co., Ltd.",
   "decision_date": "2025-02-24",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K242607",
   "device_name": "ScanDiags Ortho L-Spine MR-Q",
   "applicant": "Scandiags AG",
   "decision_date": "2025-02-21",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CH"
  },
  {
   "k_number": "K242821",
   "device_name": "EFAI Chestsuite XR Malpositioned ETT Assessment System (ETT-XR-100)",
   "applicant": "Ever Fortune.Ai, Co., Ltd.",
   "decision_date": "2025-02-20",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "TW"
  },
  {
   "k_number": "K243696",
   "device_name": "AVIEW CAC",
   "applicant": "Coreline Soft Co., Ltd.",
   "decision_date": "2025-02-14",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K250248",
   "device_name": "BriefCase-Triage",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2025-02-14",
   "product_code": "QAS",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K243250",
   "device_name": "SubtleHD (1.x)",
   "applicant": "Subtle Medical, Inc.",
   "decision_date": "2025-02-12",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K241659",
   "device_name": "Ultrasound Workspace (UWS 6.0)",
   "applicant": "Philips Ultrasound, LLC",
   "decision_date": "2025-02-10",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K241593",
   "device_name": "BoneMetrics (US)",
   "applicant": "Gleamer Sas",
   "decision_date": "2025-02-05",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K250035",
   "device_name": "Contour ProtégéAI+",
   "applicant": "Mim Software, Inc.",
   "decision_date": "2025-02-03",
   "product_code": "QKB",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K243158",
   "device_name": "TeraRecon Aorta.CT (1.1.0)",
   "applicant": "Terarecon,Inc.",
   "decision_date": "2025-01-23",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K243350",
   "device_name": "Rapid Neuro3D",
   "applicant": "Ischemaview, Inc.",
   "decision_date": "2025-01-22",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K242171",
   "device_name": "TechCare Trauma",
   "applicant": "Milvue",
   "decision_date": "2025-01-17",
   "product_code": "QBS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K243065",
   "device_name": "Cardiac Guidance",
   "applicant": "Caption Health, Inc.",
   "decision_date": "2025-01-15",
   "product_code": "QJU",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K243363",
   "device_name": "JLK-ICH",
   "applicant": "JLK, Inc.",
   "decision_date": "2025-01-03",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K242334",
   "device_name": "Ezra Flash",
   "applicant": "Ezra Ai, Inc.",
   "decision_date": "2025-01-02",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K241696",
   "device_name": "Ortho AI",
   "applicant": "Ortho Ai, LLC",
   "decision_date": "2025-01-02",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K242270",
   "device_name": "OrthoNext Platform System",
   "applicant": "Orthofix Srl",
   "decision_date": "2024-12-19",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IT"
  },
  {
   "k_number": "K243705",
   "device_name": "Saige-Density (2.5.0)",
   "applicant": "DeepHealth, Inc.",
   "decision_date": "2024-12-19",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K243688",
   "device_name": "Saige-Dx (3.1.0)",
   "applicant": "DeepHealth, Inc.",
   "decision_date": "2024-12-19",
   "product_code": "QDQ",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K240793",
   "device_name": "MSKai",
   "applicant": "Mskai",
   "decision_date": "2024-12-16",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K243548",
   "device_name": "BriefCase-Triage",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2024-12-11",
   "product_code": "QFM",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K242461",
   "device_name": "IRISeg",
   "applicant": "Intuitive Surgical, Inc.",
   "decision_date": "2024-12-10",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K242729",
   "device_name": "AutoContour (Model RADAC V4)",
   "applicant": "Radformation, Inc.",
   "decision_date": "2024-12-09",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K240680",
   "device_name": "CDM Insights",
   "applicant": "Oxford Brain Diagnostics, Ltd.",
   "decision_date": "2024-12-06",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "GB"
  },
  {
   "k_number": "K241543",
   "device_name": "DrAid™ for Liver Segmentation",
   "applicant": "Vinbrain Joint Stock Company",
   "decision_date": "2024-12-06",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "VN"
  },
  {
   "k_number": "K241923",
   "device_name": "EFAI Neurosuite CT Midline Shift Assessment System (MLS-CT-100)",
   "applicant": "Ever Fortune.Ai, Co., Ltd.",
   "decision_date": "2024-12-06",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "TW"
  },
  {
   "k_number": "K240645",
   "device_name": "Sonix Health",
   "applicant": "Ontact Health Co., Ltd.",
   "decision_date": "2024-11-27",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K241831",
   "device_name": "Transpara (2.1.0)",
   "applicant": "Screenpoint Medical B.V.",
   "decision_date": "2024-11-25",
   "product_code": "QDQ",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "NL"
  },
  {
   "k_number": "K242203",
   "device_name": "BriefCase-Quantification",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2024-11-22",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K242359",
   "device_name": "Strain AI (SAI001)",
   "applicant": "Exo, Inc.",
   "decision_date": "2024-11-20",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K241747",
   "device_name": "Saige-Dx",
   "applicant": "DeepHealth, Inc.",
   "decision_date": "2024-11-18",
   "product_code": "QDQ",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K241439",
   "device_name": "VUNO Med-Chest X-ray Triage/VUNO Med-CXR Link Triage",
   "applicant": "Vuno, Inc.",
   "decision_date": "2024-11-15",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K240417",
   "device_name": "ProFound Detection (V4.0)",
   "applicant": "Icad, Inc.",
   "decision_date": "2024-11-08",
   "product_code": "QDQ",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K240712",
   "device_name": "icobrain aria",
   "applicant": "Icometrix NV",
   "decision_date": "2024-11-07",
   "product_code": "QBS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "BE"
  },
  {
   "k_number": "K241719",
   "device_name": "NeuroICH",
   "applicant": "Neurocareai, Inc.",
   "decision_date": "2024-11-07",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K241312",
   "device_name": "TeraRecon Cardiac.Chambers.MR (1.0.0)",
   "applicant": "Terarecon,Inc.",
   "decision_date": "2024-11-05",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K241108",
   "device_name": "RemedyLogic AI MRI Lumbar Spine Reader",
   "applicant": "Remedy Logic, Inc.",
   "decision_date": "2024-10-30",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K243189",
   "device_name": "TumorSight Viz",
   "applicant": "SimBioSys, Inc.",
   "decision_date": "2024-10-25",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K242215",
   "device_name": "Neurophet AQUA (V3.1)",
   "applicant": "Neurophet., Inc.",
   "decision_date": "2024-10-25",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K241490",
   "device_name": "Contour+ (MVision AI Segmentation)",
   "applicant": "Mvision AI OY",
   "decision_date": "2024-10-18",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FI"
  },
  {
   "k_number": "K242837",
   "device_name": "BriefCase-Triage",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2024-10-18",
   "product_code": "QAS",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K242781",
   "device_name": "cvi42 Software Application",
   "applicant": "Circle Cardiovascular Imaging, Inc.",
   "decision_date": "2024-10-15",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CA"
  },
  {
   "k_number": "K241430",
   "device_name": "EchoMeasure",
   "applicant": "Icardio.Ai",
   "decision_date": "2024-10-10",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K240786",
   "device_name": "AutoChamber",
   "applicant": "HeartLung Corporation",
   "decision_date": "2024-10-10",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K241837",
   "device_name": "Limbus Contour",
   "applicant": "Limbus Ai, Inc.",
   "decision_date": "2024-10-09",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CA"
  },
  {
   "k_number": "K240553",
   "device_name": "LVivo Software Application",
   "applicant": "Dia Imaging Analysis, Ltd.",
   "decision_date": "2024-10-04",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K242652",
   "device_name": "Lunit INSIGHT DBT v1.1",
   "applicant": "Lunit, Inc.",
   "decision_date": "2024-10-04",
   "product_code": "QDQ",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K241561",
   "device_name": "MammoScreen BD",
   "applicant": "Therapixel",
   "decision_date": "2024-10-02",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K240943",
   "device_name": "LungVision",
   "applicant": "Bodyvision Medical , Ltd.",
   "decision_date": "2024-10-01",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K241480",
   "device_name": "JBS-LVO",
   "applicant": "JLK, Inc.",
   "decision_date": "2024-09-27",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K242292",
   "device_name": "uAI Easy Triage ICH",
   "applicant": "Shanghai United Imaging Intelligence Co., Ltd.",
   "decision_date": "2024-09-24",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CN"
  },
  {
   "k_number": "K240036",
   "device_name": "PIUR tUS Infinity",
   "applicant": "Piur Imaging GmbH",
   "decision_date": "2024-09-20",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "AT"
  },
  {
   "k_number": "K241280",
   "device_name": "Constellation (CON-001)",
   "applicant": "Q Bio, Inc.",
   "decision_date": "2024-09-12",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K240942",
   "device_name": "CINA-CSpine",
   "applicant": "Avicenna.Ai",
   "decision_date": "2024-09-12",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K240094",
   "device_name": "LumiNE US; Lumi",
   "applicant": "Augmedit B.V.",
   "decision_date": "2024-09-10",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "NL"
  },
  {
   "k_number": "K241681",
   "device_name": "Overjet Image Enhancement Assist",
   "applicant": "Overjet, Inc.",
   "decision_date": "2024-09-09",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K240791",
   "device_name": "ADAS 3D",
   "applicant": "Adas3D Medical S.L.",
   "decision_date": "2024-09-09",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "ES"
  },
  {
   "k_number": "K240697",
   "device_name": "See-Mode Augmented Reporting Tool, Thyroid (SMART-T)",
   "applicant": "See-Mode Technologies Pte, Ltd.",
   "decision_date": "2024-09-09",
   "product_code": "QDQ",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "SG"
  },
  {
   "k_number": "K240411",
   "device_name": "uAI Portal",
   "applicant": "Shanghai United Imaging Intelligence Co., Ltd.",
   "decision_date": "2024-09-06",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CN"
  },
  {
   "k_number": "K242300",
   "device_name": "MI View&GO",
   "applicant": "Siemens Medical Solutions USA, Inc.",
   "decision_date": "2024-08-30",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K242275",
   "device_name": "syngo.via MI Workflows; Scenium; syngo MBF",
   "applicant": "Siemens Medical Solutions USA, Inc.",
   "decision_date": "2024-08-30",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K241847",
   "device_name": "Imbio PHA (4.0.0)",
   "applicant": "Imbio, Inc.",
   "decision_date": "2024-08-30",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K241684",
   "device_name": "Overjet Charting Assist",
   "applicant": "Overjet, Inc.",
   "decision_date": "2024-08-27",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K241098",
   "device_name": "NeuroQuant",
   "applicant": "Cortechs Labs, Inc.",
   "decision_date": "2024-08-22",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K240740",
   "device_name": "qCT LN Quant",
   "applicant": "Qure.Ai Technologies",
   "decision_date": "2024-08-16",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IN"
  },
  {
   "k_number": "K241211",
   "device_name": "CoLumbo",
   "applicant": "Smart Soft Healthcare",
   "decision_date": "2024-08-15",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "BG"
  },
  {
   "k_number": "K242054",
   "device_name": "OptimMRI (v2)",
   "applicant": "Rebrain, Sas",
   "decision_date": "2024-08-12",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K233822",
   "device_name": "i2Contour",
   "applicant": "Mrimath, LLC",
   "decision_date": "2024-08-08",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K240953",
   "device_name": "AI Platform 2.0 (AIP002)",
   "applicant": "Exo Imaging",
   "decision_date": "2024-08-05",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K233984",
   "device_name": "Acumen Assisted Fluid Management (AFM) Software Feature",
   "applicant": "Edwards Lifesciences, LLC",
   "decision_date": "2024-08-02",
   "product_code": "QMS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Cardiovascular",
   "country_code": "US"
  },
  {
   "k_number": "K240301",
   "device_name": "MammoScreen® (3)",
   "applicant": "Therapixel",
   "decision_date": "2024-08-01",
   "product_code": "QDQ",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K240845",
   "device_name": "Rayvolve",
   "applicant": "Azmed Sas",
   "decision_date": "2024-07-17",
   "product_code": "QBS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K234009",
   "device_name": "Acorn 3D Software (AC-SEG-4009); Acorn 3DP Model (AC-101-XX)",
   "applicant": "Mighty Oak Medical",
   "decision_date": "2024-07-12",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K233457",
   "device_name": "RUS",
   "applicant": "Hutom, Inc.",
   "decision_date": "2024-07-12",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K241727",
   "device_name": "BriefCase-Triage",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2024-07-12",
   "product_code": "QAS",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K241329",
   "device_name": "SubtleSYNTH (1.x)",
   "applicant": "Subtle Medical, Inc.",
   "decision_date": "2024-07-11",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K240736",
   "device_name": "SMART Bun-Yo-Matic X-Ray",
   "applicant": "Disior, Ltd.",
   "decision_date": "2024-07-02",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FI"
  },
  {
   "k_number": "K240353",
   "device_name": "Hyper Insight - ICH",
   "applicant": "Sk, Inc.",
   "decision_date": "2024-07-01",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K240582",
   "device_name": "VEA Align; spineEOS",
   "applicant": "Eos Imaging",
   "decision_date": "2024-06-25",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K233196",
   "device_name": "Medihub Prostate",
   "applicant": "JLK, Inc.",
   "decision_date": "2024-06-21",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K240642",
   "device_name": "SMART Bun-Yo-Matic CT",
   "applicant": "Disior, Ltd.",
   "decision_date": "2024-06-20",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FI"
  },
  {
   "k_number": "K241083",
   "device_name": "SIS System",
   "applicant": "Surgical Information Sciences, Inc.",
   "decision_date": "2024-06-14",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K233925",
   "device_name": "Relu Creator",
   "applicant": "Relu BV",
   "decision_date": "2024-06-13",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "BE"
  },
  {
   "k_number": "K234042",
   "device_name": "EFAI Bonesuite XR Bone Age Pro Assessment System (BAP-XR-100)",
   "applicant": "Ever Fortune.Ai, Co., Ltd.",
   "decision_date": "2024-06-07",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "TW"
  },
  {
   "k_number": "K241038",
   "device_name": "Cardiac CT Function Software Application",
   "applicant": "Circle Cardiovascular Imaging",
   "decision_date": "2024-06-07",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CA"
  },
  {
   "k_number": "K240612",
   "device_name": "CINA-VCF",
   "applicant": "Avicenna.Ai",
   "decision_date": "2024-05-31",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K240769",
   "device_name": "LVivo IQS",
   "applicant": "Dia Imaging Analysis, Ltd.",
   "decision_date": "2024-05-24",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K233108",
   "device_name": "VinDr-Mammo",
   "applicant": "Vinbigdata Joint Stock Company",
   "decision_date": "2024-05-23",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "VN"
  },
  {
   "k_number": "K233209",
   "device_name": "uOmnispace.CT",
   "applicant": "Shanghai United Imaging Healthcare Co., Ltd.",
   "decision_date": "2024-05-17",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CN"
  },
  {
   "k_number": "K241112",
   "device_name": "BriefCase-Quantification",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2024-05-15",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K233247",
   "device_name": "Heuron ICH",
   "applicant": "Heuron Co., Ltd.",
   "decision_date": "2024-05-15",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K232410",
   "device_name": "SmartChest",
   "applicant": "Milvue",
   "decision_date": "2024-05-10",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K232928",
   "device_name": "DeepContour (V1.0)",
   "applicant": "Wisdom Technologies., Inc.",
   "decision_date": "2024-05-07",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CN"
  },
  {
   "k_number": "K232331",
   "device_name": "InVision Precision LVEF (LVEF)",
   "applicant": "InVision Medical Technology Corporation",
   "decision_date": "2024-04-25",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K233186",
   "device_name": "uOmnispace.MR",
   "applicant": "Shanghai United Imaging Healthcare Co., Ltd.",
   "decision_date": "2024-04-17",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CN"
  },
  {
   "k_number": "K240291",
   "device_name": "EFAI CARDIOSUITE CTA ACUTE AORTIC SYNDROME ASSESSMENT SYSTEM",
   "applicant": "Ever Fortune.Ai, Co., Ltd.",
   "decision_date": "2024-04-08",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "TW"
  },
  {
   "k_number": "K240172",
   "device_name": "Preview Shoulder",
   "applicant": "Genesis Software Innovations",
   "decision_date": "2024-04-04",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K232899",
   "device_name": "AI-Rad Companion Organs RT",
   "applicant": "Siemens Medical Solutions U.S.A.",
   "decision_date": "2024-04-03",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K233676",
   "device_name": "Us2.v2",
   "applicant": "Eko.Ai Pte Ltd. D/B/A Us2.Ai",
   "decision_date": "2024-04-01",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "SG"
  },
  {
   "k_number": "K233211",
   "device_name": "AVIEW CAC",
   "applicant": "Coreline Soft Co., Ltd.",
   "decision_date": "2024-03-29",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K232431",
   "device_name": "syngo.CT Brain Hemorrhage",
   "applicant": "Siemens Medical Solutions USA, Inc.",
   "decision_date": "2024-03-22",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K233968",
   "device_name": "CINA-iPE",
   "applicant": "Avicenna.Ai",
   "decision_date": "2024-03-13",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K233030",
   "device_name": "BoneMRI",
   "applicant": "Mriguidance B.V.",
   "decision_date": "2024-03-01",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "NL"
  },
  {
   "k_number": "K231690",
   "device_name": "iCAS-LV",
   "applicant": "Highrad , Ltd.",
   "decision_date": "2024-03-01",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K231683",
   "device_name": "inHEART Models",
   "applicant": "Inheart, Sas",
   "decision_date": "2024-02-29",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K232613",
   "device_name": "CT Cardiomegaly",
   "applicant": "Innolitics, LLC",
   "decision_date": "2024-02-28",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K233590",
   "device_name": "Overjet Charting Assist",
   "applicant": "Overjet, Inc.",
   "decision_date": "2024-02-23",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K231855",
   "device_name": "QOCA® image Smart RT Contouring System",
   "applicant": "Quanta Computer, Inc.",
   "decision_date": "2024-02-13",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "TW"
  },
  {
   "k_number": "K232363",
   "device_name": "Viz HDS, Viz Volume Plus, Viz ICH+",
   "applicant": "Viz. Ai, Inc.",
   "decision_date": "2024-02-05",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K232698",
   "device_name": "NemoScan",
   "applicant": "Software Nemotec S.L.",
   "decision_date": "2024-01-18",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "ES"
  },
  {
   "k_number": "K231871",
   "device_name": "Radify Triage",
   "applicant": "Envisionit Deepai, Ltd.",
   "decision_date": "2024-01-17",
   "product_code": "QFM",
   "clearance_type": "Abbreviated",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "GB"
  },
  {
   "k_number": "K233512",
   "device_name": "Rapid (6.0)",
   "applicant": "Ischemaview, Inc.",
   "decision_date": "2024-01-16",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K231324",
   "device_name": "DASI Dimensions (V1.0)",
   "applicant": "Dasi Simulations",
   "decision_date": "2024-01-08",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K231917",
   "device_name": "VEA Align",
   "applicant": "Eos Imaging",
   "decision_date": "2024-01-05",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K231130",
   "device_name": "TumorSight Viz",
   "applicant": "SimBioSys, Inc.",
   "decision_date": "2023-12-26",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K231929",
   "device_name": "iQ-solutions",
   "applicant": "Sydney Neuroimaging Analysis Centre Pty, Ltd.",
   "decision_date": "2023-12-18",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "AU"
  },
  {
   "k_number": "K232231",
   "device_name": "QP-Brain®",
   "applicant": "Quibim S.L.",
   "decision_date": "2023-12-13",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "ES"
  },
  {
   "k_number": "K232096",
   "device_name": "Transpara Density 1.0.0",
   "applicant": "Screenpoint Medical B.V.",
   "decision_date": "2023-12-11",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "NL"
  },
  {
   "k_number": "K223757",
   "device_name": "Bonelogic",
   "applicant": "Disior, Ltd.",
   "decision_date": "2023-12-08",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FI"
  },
  {
   "k_number": "K233568",
   "device_name": "Ceevra Reveal 3+",
   "applicant": "Ceevra, Inc.",
   "decision_date": "2023-12-05",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K232440",
   "device_name": "Adravision Perio",
   "applicant": "Adra Corporation",
   "decision_date": "2023-12-05",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K232856",
   "device_name": "Syngo Carbon Clinicals",
   "applicant": "Siemens Healthcare GmbH",
   "decision_date": "2023-12-01",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "DE"
  },
  {
   "k_number": "K232000",
   "device_name": "syngo.via MI Workflows; Scenium; syngo MBF",
   "applicant": "Siemens Medical Solutions USA, Inc.",
   "decision_date": "2023-11-28",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K232496",
   "device_name": "Brainomix 360 Triage Stroke",
   "applicant": "Brainomix Limited",
   "decision_date": "2023-11-21",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "GB"
  },
  {
   "k_number": "K232501",
   "device_name": "AI Platform (AIP001)",
   "applicant": "Exo, Inc.",
   "decision_date": "2023-11-17",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K232841",
   "device_name": "Axial3D Insight",
   "applicant": "Axial Medical Printing Limited",
   "decision_date": "2023-11-15",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "GB"
  },
  {
   "k_number": "K232083",
   "device_name": "BriefCase-Quantification",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2023-11-13",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K232257",
   "device_name": "Clarius Bladder AI",
   "applicant": "Clarius Mobile Health Corp.",
   "decision_date": "2023-11-13",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CA"
  },
  {
   "k_number": "K223754",
   "device_name": "BraveCX",
   "applicant": "Bering, Ltd.",
   "decision_date": "2023-11-09",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "GB"
  },
  {
   "k_number": "K231765",
   "device_name": "Contour ProtégéAI",
   "applicant": "Mim Software, Inc.",
   "decision_date": "2023-11-08",
   "product_code": "QKB",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K230534",
   "device_name": "BriefCase-Quantification",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2023-11-08",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K231470",
   "device_name": "Lunit INSIGHT DBT",
   "applicant": "Lunit, Inc.",
   "decision_date": "2023-11-06",
   "product_code": "QDQ",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K231955",
   "device_name": "aprevo® Digital Segmentation",
   "applicant": "Carlsmed, Inc.",
   "decision_date": "2023-11-03",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K232751",
   "device_name": "BriefCase-Triage",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2023-10-30",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K232436",
   "device_name": "Rapid SDH",
   "applicant": "Ischemaview, Inc.",
   "decision_date": "2023-10-25",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K232305",
   "device_name": "AI-Rad Companion Brain MR",
   "applicant": "Siemens Medical Solutions U.S.A.",
   "decision_date": "2023-10-23",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K230209",
   "device_name": "Sonix Health",
   "applicant": "Ontact Health Co., Ltd.",
   "decision_date": "2023-10-20",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K232367",
   "device_name": "cmAngio® V1.0",
   "applicant": "Curemetrix, Inc.",
   "decision_date": "2023-10-05",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K231398",
   "device_name": "VUNO Med-DeepBrain",
   "applicant": "Vuno, Inc.",
   "decision_date": "2023-10-04",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K231025",
   "device_name": "EFAI NeuroSuite CT ICH Assessment System",
   "applicant": "Ever Fortune.Ai, Co., Ltd.",
   "decision_date": "2023-10-04",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "TW"
  },
  {
   "k_number": "K230045",
   "device_name": "HipCheck",
   "applicant": "Stryker Corp.",
   "decision_date": "2023-09-29",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K231837",
   "device_name": "Brainomix 360 Triage LVO",
   "applicant": "Brainomix Limited",
   "decision_date": "2023-09-28",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "GB"
  },
  {
   "k_number": "K231928",
   "device_name": "EFAI RTSUITE CT HCAP-Segmentation System",
   "applicant": "Ever Fortune.Ai, Co., Ltd.",
   "decision_date": "2023-09-25",
   "product_code": "QKB",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "TW"
  },
  {
   "k_number": "K231149",
   "device_name": "qXR-CTR",
   "applicant": "Qure.Ai Technologies",
   "decision_date": "2023-09-22",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IN"
  },
  {
   "k_number": "K231384",
   "device_name": "Annalise Enterprise CTB Triage Trauma",
   "applicant": "Annalise-Ai Pty , Ltd.",
   "decision_date": "2023-09-22",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "AU"
  },
  {
   "k_number": "K231767",
   "device_name": "Annalise Enterprise CTB Triage Trauma",
   "applicant": "Annalise-Ai Pty , Ltd.",
   "decision_date": "2023-09-22",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "AU"
  },
  {
   "k_number": "K223621",
   "device_name": "DeepXray",
   "applicant": "Alpha Intelligence Manifolds, Inc.",
   "decision_date": "2023-09-08",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "TW"
  },
  {
   "k_number": "K230899",
   "device_name": "qXR-PTX-PE",
   "applicant": "Qure.Ai Technologies",
   "decision_date": "2023-08-22",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IN"
  },
  {
   "k_number": "K231094",
   "device_name": "Annalise Enterprise CTB Triage-OH",
   "applicant": "Annalise-Ai Pty , Ltd.",
   "decision_date": "2023-08-15",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "AU"
  },
  {
   "k_number": "K230074",
   "device_name": "Rapid Aneurysm Triage and Notification",
   "applicant": "Ischemaview, Inc.",
   "decision_date": "2023-07-27",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K231195",
   "device_name": "Brainomix 360 Triage ICH",
   "applicant": "Brainomix Limited",
   "decision_date": "2023-07-27",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "GB"
  },
  {
   "k_number": "K230913",
   "device_name": "ANDI",
   "applicant": "Imeka Solutions, Inc.",
   "decision_date": "2023-07-25",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CA"
  },
  {
   "k_number": "K223347",
   "device_name": "UltraSight AI Guidance",
   "applicant": "Ultrasight, Inc.",
   "decision_date": "2023-07-24",
   "product_code": "QJU",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K230150",
   "device_name": "OptimMRI",
   "applicant": "Rebrain, Sas",
   "decision_date": "2023-07-21",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K230039",
   "device_name": "uOmnispace",
   "applicant": "Shanghai United Imaging Healthcare Co., Ltd.",
   "decision_date": "2023-07-20",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CN"
  },
  {
   "k_number": "K223106",
   "device_name": "Brainlab Elements Image Fusion, Contouring (4.5);Image Fusion  (4.5);Fibertracking (2.0);BOLD MRI Mapping  (1.0);Image Fusion Angio  (1.0)",
   "applicant": "Brainlab AG",
   "decision_date": "2023-07-14",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "DE"
  },
  {
   "k_number": "K231757",
   "device_name": "Ez3D-i /E3",
   "applicant": "Ewoosoft Co., Ltd.",
   "decision_date": "2023-07-14",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K231668",
   "device_name": "Spine CAMP™ (1.1)",
   "applicant": "Medical Metrics, Inc.",
   "decision_date": "2023-07-07",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K222745",
   "device_name": "Axial3D Insight",
   "applicant": "Axial Medical Printing Limited",
   "decision_date": "2023-07-03",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "GB"
  },
  {
   "k_number": "K230497",
   "device_name": "Bladder AI (AIBV01)",
   "applicant": "Exo, Inc.",
   "decision_date": "2023-06-22",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K223556",
   "device_name": "DeepCatch",
   "applicant": "Medical IP Co., Ltd.",
   "decision_date": "2023-06-16",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K223646",
   "device_name": "IB Lab LAMA",
   "applicant": "Ib Lab GmbH",
   "decision_date": "2023-06-16",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "AT"
  },
  {
   "k_number": "K223855",
   "device_name": "FEops HEARTguideTM, FEops HEARTguideTM ALPACA",
   "applicant": "Feops NV",
   "decision_date": "2023-06-06",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "BE"
  },
  {
   "k_number": "K223491",
   "device_name": "Critical Care Suite with Pneumothorax Detection AI Algorithm, Critical Care Suite 2.1, Critical Care Suite",
   "applicant": "Ge Medical Systems, LLC",
   "decision_date": "2023-05-25",
   "product_code": "QBS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K230096",
   "device_name": "Genius AI Detection 2.0 with CC-MLO Correlation",
   "applicant": "Hologic, Inc.",
   "decision_date": "2023-05-23",
   "product_code": "QDQ",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K230082",
   "device_name": "Auto Segmentation",
   "applicant": "Ge Medical Systems, LLC",
   "decision_date": "2023-05-04",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K230977",
   "device_name": "SIS System",
   "applicant": "Surgical Information Sciences, Inc.",
   "decision_date": "2023-05-02",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K222676",
   "device_name": "Ceevra Reveal 3",
   "applicant": "Ceevra, Inc.",
   "decision_date": "2023-04-25",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K223501",
   "device_name": "ViewFinder Software Version 1.1",
   "applicant": "Elaitra, Ltd.",
   "decision_date": "2023-04-21",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "GB"
  },
  {
   "k_number": "K230023",
   "device_name": "ART-Plan",
   "applicant": "Therapanacea Sas",
   "decision_date": "2023-04-19",
   "product_code": "QKB",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K230685",
   "device_name": "AutoContour Model RADAC V3",
   "applicant": "Radformation, Inc.",
   "decision_date": "2023-04-14",
   "product_code": "QKB",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K213986",
   "device_name": "CerebralGo Plus",
   "applicant": "Yukun (Beijing) Technology Co., Ltd.",
   "decision_date": "2023-04-13",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CN"
  },
  {
   "k_number": "K223774",
   "device_name": "Contour ProtégéAI",
   "applicant": "Mim Software, Inc.",
   "decision_date": "2023-04-06",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K223240",
   "device_name": "Annalise Enterprise CTB Triage Trauma",
   "applicant": "Annalise-Ai Pty , Ltd.",
   "decision_date": "2023-04-03",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "AU"
  },
  {
   "k_number": "K213272",
   "device_name": "Formus Hip",
   "applicant": "Formus Labs, Ltd.",
   "decision_date": "2023-03-31",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "NZ"
  },
  {
   "k_number": "K222174",
   "device_name": "RadioLens v1.0",
   "applicant": "Synapsica",
   "decision_date": "2023-03-28",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K222179",
   "device_name": "Annalise Enterprise CXR Triage Trauma",
   "applicant": "Annalise-Ai Pty , Ltd.",
   "decision_date": "2023-03-28",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "AU"
  },
  {
   "k_number": "K222268",
   "device_name": "Annalise Enterprise CXR Triage Trauma",
   "applicant": "Annalise-Ai Pty , Ltd.",
   "decision_date": "2023-03-28",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "AU"
  },
  {
   "k_number": "K222036",
   "device_name": "MPXA-2000",
   "applicant": "Medipixel, Inc.",
   "decision_date": "2023-03-22",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K223443",
   "device_name": "Viz AAA",
   "applicant": "Viz. Ai, Inc.",
   "decision_date": "2023-03-17",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K221706",
   "device_name": "AccuContour",
   "applicant": "Manteia Technologies Co., Ltd.",
   "decision_date": "2023-03-09",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CN"
  },
  {
   "k_number": "K222176",
   "device_name": "BoneView",
   "applicant": "Gleamer",
   "decision_date": "2023-03-02",
   "product_code": "QBS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K222884",
   "device_name": "Rapid NCCT Stroke",
   "applicant": "Ischemaview, Inc.",
   "decision_date": "2023-03-02",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "DEN220063",
   "device_name": "Caption Interpretation Automated Ejection Fraction Software",
   "applicant": "Caption Health, Inc.",
   "decision_date": "2023-02-24",
   "product_code": "QVD",
   "clearance_type": "Direct",
   "decision_description": "Unknown",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K230197",
   "device_name": "BoneMRI v1.6",
   "applicant": "Mriguidance B.V.",
   "decision_date": "2023-02-22",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "NL"
  },
  {
   "k_number": "K223296",
   "device_name": "Videa Perio Assist",
   "applicant": "Videahealth, Inc.",
   "decision_date": "2023-02-06",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K223396",
   "device_name": "Rapid RV/LV",
   "applicant": "Ischemaview, Inc.",
   "decision_date": "2023-02-01",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K222970",
   "device_name": "LVivo IQS",
   "applicant": "Dia Imaging Analysis, Ltd.",
   "decision_date": "2023-02-01",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K230020",
   "device_name": "BriefCase",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2023-02-01",
   "product_code": "QFM",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K221868",
   "device_name": "QOCA image Smart CXR Image Processing System",
   "applicant": "Quanta Computer, Inc.",
   "decision_date": "2023-01-27",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "TW"
  },
  {
   "k_number": "K222406",
   "device_name": "Clarius AI",
   "applicant": "Clarius Mobile Health Corp.",
   "decision_date": "2023-01-23",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CA"
  },
  {
   "k_number": "K214036",
   "device_name": "AVIEW",
   "applicant": "Coreline Soft Co., Ltd.",
   "decision_date": "2022-12-23",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K222275",
   "device_name": "Saige-Density",
   "applicant": "DeepHealth, Inc.",
   "decision_date": "2022-12-16",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K223268",
   "device_name": "BrainInsight",
   "applicant": "Hyperfine, Inc.",
   "decision_date": "2022-12-16",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K222692",
   "device_name": "BriefCase",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2022-12-05",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K221716",
   "device_name": "CINA",
   "applicant": "Avicenna.Ai",
   "decision_date": "2022-11-22",
   "product_code": "QAS",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K223032",
   "device_name": "SIS System (Version 5.6.0)",
   "applicant": "Surgical Information Sciences, Inc.",
   "decision_date": "2022-11-21",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K221330",
   "device_name": "BriefCase",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2022-11-18",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K221762",
   "device_name": "BoneMRI v1.4",
   "applicant": "Mrlguidance B.V.",
   "decision_date": "2022-11-16",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "NL"
  },
  {
   "k_number": "K222428",
   "device_name": "Syngo Dynamics (Version VA40F)",
   "applicant": "Siemens Medical Solutions USA, Inc.",
   "decision_date": "2022-11-14",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K220408",
   "device_name": "AVIEW RT ACS",
   "applicant": "Coreline Soft Co., Ltd.",
   "decision_date": "2022-11-10",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K221552",
   "device_name": "EFAI ChestSuite XR Pneumothorax Assessment System",
   "applicant": "Ever Fortune.Ai, Co., Ltd.",
   "decision_date": "2022-11-08",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "TW"
  },
  {
   "k_number": "K223042",
   "device_name": "Viz LVO ContaCT",
   "applicant": "Viz. Ai, Inc.",
   "decision_date": "2022-10-21",
   "product_code": "QAS",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K221632",
   "device_name": "Spine CAMP™",
   "applicant": "Medical Metrics, Inc.",
   "decision_date": "2022-10-18",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K221305",
   "device_name": "AI-Rad Companion Organs RT",
   "applicant": "Siemens Medical Solutions USA, Inc.",
   "decision_date": "2022-10-14",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K220709",
   "device_name": "BriefCase",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2022-10-07",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K221449",
   "device_name": "Genius AI Detection 2.0",
   "applicant": "Hologic, Inc.",
   "decision_date": "2022-10-06",
   "product_code": "QDQ",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K211611",
   "device_name": "QIR Suite",
   "applicant": "Casis Cardiac Simulation & Imaging Software",
   "decision_date": "2022-09-30",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K220080",
   "device_name": "CogNet QmTRIAGE",
   "applicant": "Medcognetics, Inc.",
   "decision_date": "2022-09-29",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K222329",
   "device_name": "BriefCase",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2022-09-28",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K221738",
   "device_name": "NS-HGlio",
   "applicant": "Neosoma, Inc.",
   "decision_date": "2022-09-27",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K221456",
   "device_name": "Rapid ICH",
   "applicant": "Ischemaview, Inc.",
   "decision_date": "2022-09-12",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K222076",
   "device_name": "EFAI ChestSuite XR Pleural Effusion Assessment System",
   "applicant": "Ever Fortune.Ai, Co., Ltd.",
   "decision_date": "2022-09-08",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "TW"
  },
  {
   "k_number": "K221241",
   "device_name": "DrAid for Radiology v1",
   "applicant": "Vinbrain Joint Stock Company",
   "decision_date": "2022-09-01",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "VN"
  },
  {
   "k_number": "K221100",
   "device_name": "Viz RV/LV",
   "applicant": "Viz. Ai, Inc.",
   "decision_date": "2022-08-29",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K222277",
   "device_name": "BriefCase",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2022-08-26",
   "product_code": "QAS",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K220598",
   "device_name": "AutoContour Model RADAC V2",
   "applicant": "Radformation, Inc.",
   "decision_date": "2022-08-24",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K222172",
   "device_name": "MI View&GO",
   "applicant": "Siemens Medical Solutions USA, Inc.",
   "decision_date": "2022-08-19",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K213645",
   "device_name": "ClearPoint Maestro Brain Model",
   "applicant": "ClearPoint Neuro, Inc.",
   "decision_date": "2022-08-08",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K221432",
   "device_name": "Customize",
   "applicant": "3D-Side S.A.",
   "decision_date": "2022-08-03",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "BE"
  },
  {
   "k_number": "K221347",
   "device_name": "Transpara 1.7.2",
   "applicant": "Screenpoint Medical B.V.",
   "decision_date": "2022-08-03",
   "product_code": "QDQ",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "NL"
  },
  {
   "k_number": "K213998",
   "device_name": "cvi42 Auto Imaging Software Application",
   "applicant": "Circle Cardiovascular Imaging, Inc.",
   "decision_date": "2022-07-28",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CA"
  },
  {
   "k_number": "K220439",
   "device_name": "Viz SDH",
   "applicant": "Viz. Ai, Inc.",
   "decision_date": "2022-07-25",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K220940",
   "device_name": "EchoPAC Software Only, EchoPAC Plug-in",
   "applicant": "GE Medical Systems Ultrasound and Primary Care Diagnostics",
   "decision_date": "2022-07-22",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K220956",
   "device_name": "Libby Echo:Prio",
   "applicant": "Dyad Medical, Inc.",
   "decision_date": "2022-07-20",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K220815",
   "device_name": "BrainInsight",
   "applicant": "Hyperfine, Inc.",
   "decision_date": "2022-07-19",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K212783",
   "device_name": "ProstatID",
   "applicant": "Scanmed, LLC",
   "decision_date": "2022-07-08",
   "product_code": "QDQ",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K220497",
   "device_name": "CoLumbo",
   "applicant": "Smart Soft Healthcare AD",
   "decision_date": "2022-06-23",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "BG"
  },
  {
   "k_number": "K220813",
   "device_name": "ART-PLAN",
   "applicant": "Therapanacea",
   "decision_date": "2022-06-17",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K221314",
   "device_name": "BriefCase",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2022-06-03",
   "product_code": "QAS",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K220164",
   "device_name": "Rayvolve",
   "applicant": "Azmed Sas",
   "decision_date": "2022-06-02",
   "product_code": "QBS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K221248",
   "device_name": "Rapid LVO",
   "applicant": "Ischemaview, Inc.",
   "decision_date": "2022-05-31",
   "product_code": "QAS",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K220499",
   "device_name": "Rapid PE Triage and Notification (PETN)",
   "applicant": "Ischemaview, Inc.",
   "decision_date": "2022-05-17",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K221240",
   "device_name": "BriefCase",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2022-05-17",
   "product_code": "QAS",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K220105",
   "device_name": "Saige-Dx",
   "applicant": "DeepHealth, Inc.",
   "decision_date": "2022-05-12",
   "product_code": "QDQ",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K212915",
   "device_name": "MVision AI Segmentation",
   "applicant": "MVision AI",
   "decision_date": "2022-05-03",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FI"
  },
  {
   "k_number": "K220264",
   "device_name": "EFAI RTSuite CT HN-Segmentation System",
   "applicant": "Ever Fortune.Ai, Co., Ltd.",
   "decision_date": "2022-04-28",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "TW"
  },
  {
   "k_number": "K213886",
   "device_name": "BriefCase",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2022-04-26",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K213706",
   "device_name": "AI-Rad Companion Brain MR",
   "applicant": "Siemens Healthcare GmbH",
   "decision_date": "2022-04-15",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K212624",
   "device_name": "EFAI Intelligent Cardiothoracic Ratio (iCTR) Assessment System",
   "applicant": "Ever Fortune.Ai, Co., Ltd.",
   "decision_date": "2022-04-04",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "TW"
  },
  {
   "k_number": "K213721",
   "device_name": "BriefCase",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2022-03-21",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K213779",
   "device_name": "Customize",
   "applicant": "3D-Side S.A.",
   "decision_date": "2022-03-16",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "BE"
  },
  {
   "k_number": "K203744",
   "device_name": "Arterys MICA",
   "applicant": "Arterys, Inc.",
   "decision_date": "2022-03-14",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K214043",
   "device_name": "BriefCase",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2022-03-14",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K213566",
   "device_name": "ClearRead Xray Pneumothorax",
   "applicant": "Riverain Technologies, Inc.",
   "decision_date": "2022-03-10",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K212365",
   "device_name": "BoneView",
   "applicant": "Gleamer",
   "decision_date": "2022-03-01",
   "product_code": "QBS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K213941",
   "device_name": "Annalise Enterprise CXR Triage Pneumothorax",
   "applicant": "Annalise-Ai",
   "decision_date": "2022-02-24",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "AU"
  },
  {
   "k_number": "K213319",
   "device_name": "Viz ANEURYSM, Viz ANX",
   "applicant": "Viz. Ai, Inc.",
   "decision_date": "2022-02-18",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K213976",
   "device_name": "Contour ProtégéAI",
   "applicant": "Mim Software, Inc.",
   "decision_date": "2022-02-03",
   "product_code": "QKB",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K203260",
   "device_name": "syngo.CT Brain Hemorrhage",
   "applicant": "Siemens Medical Solutions USA, Inc.",
   "decision_date": "2022-01-28",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K212012",
   "device_name": "Follicle Clarity",
   "applicant": "Cycle Clarity",
   "decision_date": "2022-01-19",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K210747",
   "device_name": "Caption Interpretation Automated Ejection Fraction Software",
   "applicant": "Caption Health",
   "decision_date": "2022-01-19",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K213544",
   "device_name": "TOMTEC-ARENA",
   "applicant": "Tomtec Imaging Systems GmbH",
   "decision_date": "2022-01-06",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "DE"
  },
  {
   "k_number": "K202404",
   "device_name": "BoneMRI",
   "applicant": "Mriguidance B.V.",
   "decision_date": "2021-12-22",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "NL"
  },
  {
   "k_number": "K212690",
   "device_name": "qXR-BT",
   "applicant": "Qure.Ai Technologies",
   "decision_date": "2021-12-21",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IN"
  },
  {
   "k_number": "K210670",
   "device_name": "BU-CAD",
   "applicant": "Taihao Medical, Inc.",
   "decision_date": "2021-12-21",
   "product_code": "QDQ",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "TW"
  },
  {
   "k_number": "K213275",
   "device_name": "EchoGo Core (2.0)",
   "applicant": "Ultromics Limited",
   "decision_date": "2021-12-20",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "GB"
  },
  {
   "k_number": "K213628",
   "device_name": "VBrain",
   "applicant": "Vysioneer, Inc.",
   "decision_date": "2021-12-16",
   "product_code": "QKB",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K213155",
   "device_name": "RT-Mind-AI",
   "applicant": "Medmind Technology Co., Ltd.",
   "decision_date": "2021-12-15",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CN"
  },
  {
   "k_number": "K211803",
   "device_name": "HealthPPT",
   "applicant": "Zebra Medical Vision, Ltd.",
   "decision_date": "2021-12-15",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K212466",
   "device_name": "LVivo Seamless",
   "applicant": "Dia Imaging Analysis, Ltd.",
   "decision_date": "2021-12-09",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K211541",
   "device_name": "MammoScreen 2.0",
   "applicant": "Therapixel",
   "decision_date": "2021-11-26",
   "product_code": "QDQ",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K210831",
   "device_name": "OnQ Neuro",
   "applicant": "Cortechs Labs, Inc.",
   "decision_date": "2021-11-19",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K211678",
   "device_name": "Lunit INSIGHT MMG",
   "applicant": "Lunit, Inc.",
   "decision_date": "2021-11-17",
   "product_code": "QDQ",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K211733",
   "device_name": "Lunit INSIGHT CXR Triage",
   "applicant": "Lunit, Inc.",
   "decision_date": "2021-11-10",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K211161",
   "device_name": "Critical Care Suite with Endotracheal Tube Positing AI algorithm",
   "applicant": "Ge Medical Systems, LLC",
   "decision_date": "2021-10-29",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K212218",
   "device_name": "Advanced Algorithms for Treatment Management Applications (AATMA)",
   "applicant": "Elekta Solutions AB",
   "decision_date": "2021-10-25",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "SE"
  },
  {
   "k_number": "K210632",
   "device_name": "Contour ProtegeAI",
   "applicant": "Mim Software, Inc.",
   "decision_date": "2021-10-20",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K212261",
   "device_name": "StrokeSENS LVO",
   "applicant": "Circle Neurovascular Imaging, Inc.",
   "decision_date": "2021-10-14",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CA"
  },
  {
   "k_number": "K212116",
   "device_name": "VBrain-OAR",
   "applicant": "Vysioneer, Inc.",
   "decision_date": "2021-10-12",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K203785",
   "device_name": "ClariSIGMAM",
   "applicant": "Claripi, Inc.",
   "decision_date": "2021-09-10",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "KR"
  },
  {
   "k_number": "K203555",
   "device_name": "AmCAD-UT",
   "applicant": "Amcad Biomed Corporation",
   "decision_date": "2021-09-08",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "TW"
  },
  {
   "k_number": "K211179",
   "device_name": "InferRead CT Stroke.AI",
   "applicant": "Infervision Medical Technology Co., Ltd.",
   "decision_date": "2021-08-12",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CN"
  },
  {
   "k_number": "K211431",
   "device_name": "breastscape v1.0",
   "applicant": "Olea Medical",
   "decision_date": "2021-08-02",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K211222",
   "device_name": "qER-Quant",
   "applicant": "Qure.Ai Technologies",
   "decision_date": "2021-07-30",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IN"
  },
  {
   "k_number": "K210791",
   "device_name": "Us2.v1",
   "applicant": "Eko.Ai Pte Ltd. D/B/A Us2.Ai",
   "decision_date": "2021-07-27",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "SG"
  },
  {
   "k_number": "K210719",
   "device_name": "Change Healthcare Anatomical AI",
   "applicant": "Change Healthcare Canada Company",
   "decision_date": "2021-07-20",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CA"
  },
  {
   "k_number": "K211506",
   "device_name": "PowerLook Density Assessment V4.0",
   "applicant": "Icad, Inc.",
   "decision_date": "2021-07-12",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K211788",
   "device_name": "HALO",
   "applicant": "Nicolab B.V.",
   "decision_date": "2021-07-08",
   "product_code": "QAS",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "NL"
  },
  {
   "k_number": "K211459",
   "device_name": "syngo.via MI WorkFlows, Scenium, syngo MBF",
   "applicant": "Siemens Medical Solutions USA, Inc.",
   "decision_date": "2021-06-10",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K210404",
   "device_name": "Transpara 1.7.0",
   "applicant": "Screenpoint Medical B.V.",
   "decision_date": "2021-06-02",
   "product_code": "QDQ",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "NL"
  },
  {
   "k_number": "K210237",
   "device_name": "CINA CHEST",
   "applicant": "Avicenna.Ai",
   "decision_date": "2021-05-19",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K203502",
   "device_name": "MEDO-Thyroid",
   "applicant": "Medo DX Pte. , Ltd.",
   "decision_date": "2021-04-23",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CA"
  },
  {
   "k_number": "K210556",
   "device_name": "Preview Shoulder",
   "applicant": "Genesis Software Innovations",
   "decision_date": "2021-04-21",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K203610",
   "device_name": "Automatic Anatomy Recognition (AAR)",
   "applicant": "Quantitative Radiology Solutions, LLC",
   "decision_date": "2021-04-20",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K203517",
   "device_name": "Saige-Q",
   "applicant": "DeepHealth, Inc.",
   "decision_date": "2021-04-16",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K202992",
   "device_name": "BriefCase, RIB Fractures Triage (RibFx)",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2021-04-14",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K202928",
   "device_name": "DV. Target",
   "applicant": "Deepvoxel, Inc.",
   "decision_date": "2021-04-02",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K210209",
   "device_name": "Viz ICH",
   "applicant": "Viz. Ai, Inc.",
   "decision_date": "2021-03-23",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K203235",
   "device_name": "VBrain",
   "applicant": "Vysioneer, Inc.",
   "decision_date": "2021-03-19",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K203822",
   "device_name": "ProFound AI Software V3.0",
   "applicant": "Icad, Inc.",
   "decision_date": "2021-03-12",
   "product_code": "QDQ",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K203256",
   "device_name": "Imbio RV/LV Software",
   "applicant": "Imbio, LLC",
   "decision_date": "2021-03-09",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K210053",
   "device_name": "LVivo Software Application",
   "applicant": "Dia Imaging Analysis, Ltd.",
   "decision_date": "2021-02-05",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K201411",
   "device_name": "Visage Breast Density",
   "applicant": "Visage Imaging GmbH",
   "decision_date": "2021-01-29",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "DE"
  },
  {
   "k_number": "K193271",
   "device_name": "uAI EasyTriage-Rib",
   "applicant": "Shanghai United Imaging Intelligence Co., Ltd.",
   "decision_date": "2021-01-15",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CN"
  },
  {
   "k_number": "K202700",
   "device_name": "ART-Plan",
   "applicant": "Therapanacea",
   "decision_date": "2021-01-14",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K203508",
   "device_name": "BriefCase",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2020-12-29",
   "product_code": "QAS",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K200873",
   "device_name": "HALO",
   "applicant": "Nico-Lab B.V.",
   "decision_date": "2020-11-20",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "NL"
  },
  {
   "k_number": "K201195",
   "device_name": "syngo.via MI Workflows, syngo MBF",
   "applicant": "Siemens Medical Solutions USA, Inc.",
   "decision_date": "2020-11-18",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K201019",
   "device_name": "Genius AI Detection",
   "applicant": "Hologic, Inc.",
   "decision_date": "2020-11-18",
   "product_code": "QDQ",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "DEN190029",
   "device_name": "Acumen Assisted Fluid Management (AFM) Software Feature",
   "applicant": "Edwards Lifesciences",
   "decision_date": "2020-11-13",
   "product_code": "QMS",
   "clearance_type": "Direct",
   "decision_description": "Unknown",
   "advisory_committee": "Cardiovascular",
   "country_code": "US"
  },
  {
   "k_number": "K193562",
   "device_name": "AI-Rad Companion Organs RT",
   "applicant": "Siemens Medical Solutions USA, Inc.",
   "decision_date": "2020-11-06",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K200323",
   "device_name": "AutoContour",
   "applicant": "Radformation, Inc.",
   "decision_date": "2020-10-30",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K202013",
   "device_name": "WRDensity by Whiterabbit.ai",
   "applicant": "Whiterabbit.Ai, Inc.",
   "decision_date": "2020-10-30",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K202546",
   "device_name": "LVivo Seamless",
   "applicant": "Dia Imaging Analysis, Ltd.",
   "decision_date": "2020-09-29",
   "product_code": "QIH",
   "clearance_type": "Special",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K201992",
   "device_name": "Caption Guidance",
   "applicant": "Caption Health",
   "decision_date": "2020-09-18",
   "product_code": "QJU",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K201020",
   "device_name": "BriefCase",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2020-08-26",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K201310",
   "device_name": "Accipiolx",
   "applicant": "Maxq AL , Ltd.",
   "decision_date": "2020-08-07",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K193283",
   "device_name": "AI-Rad Companion Prostate MR",
   "applicant": "Siemens Medical Solutions USA, Inc.",
   "decision_date": "2020-07-30",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K193417",
   "device_name": "FractureDetect (FX)",
   "applicant": "Imagen Technologies, Inc.",
   "decision_date": "2020-07-30",
   "product_code": "QBS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K200621",
   "device_name": "Caption Interpretation Automated Ejection Fraction Software",
   "applicant": "Caption Health",
   "decision_date": "2020-07-22",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K200905",
   "device_name": "HealthMammo",
   "applicant": "Zebra Medical Vision, Ltd.",
   "decision_date": "2020-07-16",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K192969",
   "device_name": "Ezra Plexo Software",
   "applicant": "Ezra Ai, Inc.",
   "decision_date": "2020-07-10",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K200941",
   "device_name": "Rapid LVO",
   "applicant": "Ischemaview, Inc.",
   "decision_date": "2020-07-09",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K193252",
   "device_name": "Contour ProtegeAI",
   "applicant": "Mim Software, Inc.",
   "decision_date": "2020-07-02",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K200855",
   "device_name": "CINA",
   "applicant": "Avicenna.Ai",
   "decision_date": "2020-06-24",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K200232",
   "device_name": "LVivo Software Application",
   "applicant": "Dia Imaging Analysis, Ltd.",
   "decision_date": "2020-06-23",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K193298",
   "device_name": "BriefCase",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2020-06-19",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K200921",
   "device_name": "qER",
   "applicant": "Qure.Ai Technologies",
   "decision_date": "2020-06-17",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IN"
  },
  {
   "k_number": "K200356",
   "device_name": "MEDO ARIA",
   "applicant": "Medo.Ai",
   "decision_date": "2020-06-11",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CA"
  },
  {
   "k_number": "K200974",
   "device_name": "QLAB Advanced Quantification Software",
   "applicant": "Philips Health Care",
   "decision_date": "2020-06-03",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K192601",
   "device_name": "uWS-MR",
   "applicant": "Shanghai United Imaging Healthcare Co., Ltd.",
   "decision_date": "2020-06-01",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CN"
  },
  {
   "k_number": "K192901",
   "device_name": "HealthVCF",
   "applicant": "Zebra Medical Vision, Ltd.",
   "decision_date": "2020-05-12",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K193351",
   "device_name": "NinesAI",
   "applicant": "Nines, Inc.",
   "decision_date": "2020-04-21",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K200755",
   "device_name": "Caption Guidance",
   "applicant": "Caption Health",
   "decision_date": "2020-04-16",
   "product_code": "QJU",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K192167",
   "device_name": "CuraRad-ICH",
   "applicant": "Curacloud Corp.",
   "decision_date": "2020-04-13",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K193300",
   "device_name": "AIMI-Triage CXR PTX",
   "applicant": "Radlogics, Inc.",
   "decision_date": "2020-04-08",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K193087",
   "device_name": "Rapid ICH",
   "applicant": "Ischemaview Incorporated",
   "decision_date": "2020-03-31",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K192437",
   "device_name": "Arterys MICA",
   "applicant": "Arterys, Inc.",
   "decision_date": "2020-03-25",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K192854",
   "device_name": "MammoScreen",
   "applicant": "Therapixel",
   "decision_date": "2020-03-25",
   "product_code": "QDQ",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "FR"
  },
  {
   "k_number": "K193658",
   "device_name": "Viz ICH",
   "applicant": "Viz. Ai, Inc.",
   "decision_date": "2020-03-18",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K193229",
   "device_name": "Transpara",
   "applicant": "Screenpoint Medical B.V.",
   "decision_date": "2020-03-05",
   "product_code": "QDQ",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "NL"
  },
  {
   "k_number": "K191928",
   "device_name": "AccuContour",
   "applicant": "Xiamen Manteia Technology , Ltd.",
   "decision_date": "2020-02-28",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "CN"
  },
  {
   "k_number": "K191556",
   "device_name": "Red Dot",
   "applicant": "Behold.Ai Technologies Limited",
   "decision_date": "2020-02-28",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "GB"
  },
  {
   "k_number": "DEN190040",
   "device_name": "Caption Guidance",
   "applicant": "Bay Labs, Inc.",
   "decision_date": "2020-02-07",
   "product_code": "QJU",
   "clearance_type": "Direct",
   "decision_description": "Unknown",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K191647",
   "device_name": "QLAB Advanced Quantification Software",
   "applicant": "Philips Health Care",
   "decision_date": "2019-12-20",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K192383",
   "device_name": "BriefCase",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2019-12-20",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K192287",
   "device_name": "Transpara",
   "applicant": "Screenpoint Medical B.V.",
   "decision_date": "2019-12-10",
   "product_code": "QDQ",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "NL"
  },
  {
   "k_number": "K192320",
   "device_name": "HealthCXR",
   "applicant": "Zebra Medical Vision, Ltd.",
   "decision_date": "2019-11-26",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K191171",
   "device_name": "EchoGo Core",
   "applicant": "Ultromics, Ltd.",
   "decision_date": "2019-11-13",
   "product_code": "QIH",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "GB"
  },
  {
   "k_number": "K191994",
   "device_name": "ProFound AI Software V2.1",
   "applicant": "Icad, Inc.",
   "decision_date": "2019-10-04",
   "product_code": "QDQ",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K183182",
   "device_name": "Critical Care Suite",
   "applicant": "Ge Medical Systems, LLC",
   "decision_date": "2019-08-12",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K182875",
   "device_name": "DeepCT",
   "applicant": "Deep01 Limited",
   "decision_date": "2019-07-10",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "TW"
  },
  {
   "k_number": "K190424",
   "device_name": "HealthICH",
   "applicant": "Zebra Medical Vision, Ltd.",
   "decision_date": "2019-06-13",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K190896",
   "device_name": "BriefCase",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2019-05-31",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K190362",
   "device_name": "HealthPNX",
   "applicant": "Zebra Medical Vision, Ltd.",
   "decision_date": "2019-05-06",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K190072",
   "device_name": "BriefCase",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2019-04-15",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K183285",
   "device_name": "cmTriage",
   "applicant": "Curemetrix, Inc.",
   "decision_date": "2019-03-08",
   "product_code": "QFM",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K182373",
   "device_name": "PowerLook Tomo Detection V2 Software",
   "applicant": "Icad, Inc.",
   "decision_date": "2018-12-06",
   "product_code": "QDQ",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "K181704",
   "device_name": "Transpara",
   "applicant": "Screenpoint Medical B.V.",
   "decision_date": "2018-11-21",
   "product_code": "QDQ",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "NL"
  },
  {
   "k_number": "K182177",
   "device_name": "Accipiolx",
   "applicant": "Maxq-Al , Ltd.",
   "decision_date": "2018-10-26",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K180647",
   "device_name": "BriefCase",
   "applicant": "Aidoc Medical , Ltd.",
   "decision_date": "2018-08-01",
   "product_code": "QAS",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "IL"
  },
  {
   "k_number": "K181572",
   "device_name": "Workflow Box",
   "applicant": "Mirada Medical, Ltd.",
   "decision_date": "2018-07-10",
   "product_code": "QKB",
   "clearance_type": "Traditional",
   "decision_description": "Substantially Equivalent",
   "advisory_committee": "Radiology",
   "country_code": "GB"
  },
  {
   "k_number": "DEN180005",
   "device_name": "OsteoDetect",
   "applicant": "Imagen Technologies, Inc.",
   "decision_date": "2018-05-24",
   "product_code": "QBS",
   "clearance_type": "Direct",
   "decision_description": "Unknown",
   "advisory_committee": "Radiology",
   "country_code": "US"
  },
  {
   "k_number": "DEN170073",
   "device_name": "ContaCT",
   "applicant": "Viz.Al, Inc.",
   "decision_date": "2018-02-13",
   "product_code": "QAS",
   "clearance_type": "Direct",
   "decision_description": "Unknown",
   "advisory_committee": "Radiology",
   "country_code": "US"
  }
 ]
}