510(k) K132083 ยท KRD Device, Vascular, For Promoting Embolization
AZUR PURE PERIPHERAL COIL SYSTEMS, PUSHABLE 35
| Applicant | MicroVention, Inc., Tistin CA, US |
| Decision | Substantially Equivalent, Oct 28, 2013 |
| Received | Jul 5, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132083
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.