510(k) K111307 ยท KRD Device, Vascular, For Promoting Embolization
AZUR DETACHABLE 35 PLATINUM COIL SYSTEM
| Applicant | MicroVention, Inc., Tistin CA, US |
| Decision | Substantially Equivalent, Jun 15, 2011 |
| Received | May 10, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K111307
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.