Transparency Registry · K230685
AutoContour Model RADAC V3
Radformation, Inc. · cleared 2023-04-14 under product code QKB (Radiological Image Processing Software For Radiation Therapy).
The public record
| 510(k) number | K230685 (FDA database) |
| Device name as cleared | AutoContour Model RADAC V3 |
| Applicant | Radformation, Inc. (New York, NY, US) |
| Decision | Substantially Equivalent · Special pathway |
| Decision date | 2023-04-14 |
| FDA product code | QKB — Radiological Image Processing Software For Radiation Therapy |
| Review panel | Radiology |
Source: openFDA 510(k) records, stored verbatim. Entry added 2026-08-29; the source link above is authoritative if any discrepancy exists.
Public disclosure beyond the clearance
| FDA clearance record | Located — linked above |
| Public model card / intended-use document | Not yet located in public sources |
| Peer-reviewed validation publication | Not yet located in public sources |
| Published subgroup / equity performance | Not yet located in public sources |
| Public monitoring or update commitments | Not yet located in public sources |
"Not yet located" is a statement about what we could find in public sources — not a statement about the product or whether such materials exist privately. Vendors: these rows update free of charge on submission of a public link — start here.
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