icobrain aria is an AI-enabled medical device from icometrix NV, listed by FDA (510(k), K240712) with a decision date of 2024-11-07. Review panel: Radiology.
| FDA submission number | K240712 |
|---|---|
| Pathway | 510(k) |
| Company | icometrix NV |
| Review panel (specialty) | Radiology |
| FDA decision date | 2024-11-07 |
| Decision | Substantially Equivalent |
| Product code | QBS |
| Classification | Radiological Computer Assisted Detection/Diagnosis Software For Fracture |
| Device class | 2 |
| Regulation number | 892.2090 |
| Review time (calendar days) | 237 |
| Applicant country | BE |
Official FDA database record · FDA AI-enabled device list
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Data from FDA's AI-enabled device list and openFDA. Informational only; verify against the FDA record.