510(k) K162524 ยท KRD Device, Vascular, For Promoting Embolization
AZUR CX Detachable 18 Peripheral Coil System
| Applicant | MicroVention, Inc., Tistin CA, US |
| Decision | Substantially Equivalent, Mar 3, 2017 |
| Received | Sep 9, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162524
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.