510(k) K212442 ยท OWB Interventional Fluoroscopic X-Ray System
Cydar EV (Series B) and Cydar EV Maps
| Applicant | Cydar , Ltd., Barrington, GB |
| Decision | Substantially Equivalent, Dec 3, 2021 |
| Received | Aug 4, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212442
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.