510(k) K122316 ยท KRD Device, Vascular, For Promoting Embolization
AZUR DETACHABLE 35
| Applicant | MicroVention, Inc., Tistin CA, US |
| Decision | Substantially Equivalent, Aug 29, 2012 |
| Received | Aug 1, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K122316
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.