510(k) K123384 ยท KRD Device, Vascular, For Promoting Embolization
AZUR CX DETACHABLE 18
| Applicant | MicroVention, Inc., Tistin CA, US |
| Decision | Substantially Equivalent, Nov 28, 2012 |
| Received | Nov 2, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K123384
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.