510(k) K091882 ยท KRD Device, Vascular, For Promoting Embolization
AZUR PERIPHERAL HYDROCOIL ENDOVASCULAR EMBOLIZATION SYSTEM
| Applicant | MicroVention, Inc., Aliso Viejo CA, US |
| Decision | Substantially Equivalent, Jul 8, 2009 |
| Received | Jun 24, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K091882
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.