Cydar EV (Series B) and Cydar EV Maps is an AI-enabled medical device from Cydar Ltd., listed by FDA (510(k), K212442) with a decision date of 2021-12-03. Review panel: Radiology.
| FDA submission number | K212442 |
|---|---|
| Pathway | 510(k) |
| Company | Cydar Ltd. |
| Review panel (specialty) | Radiology |
| FDA decision date | 2021-12-03 |
| Decision | Substantially Equivalent |
| Product code | OWB |
| Classification | Interventional Fluoroscopic X-Ray System |
| Device class | 2 |
| Regulation number | 892.1650 |
| Review time (calendar days) | 121 |
| Applicant country | GB |
Official FDA database record · FDA AI-enabled device list
All Radiology AI devices · Full device index
Data from FDA's AI-enabled device list and openFDA. Informational only; verify against the FDA record.