510(k) K130577 ยท KRD Device, Vascular, For Promoting Embolization
AZUR PUSHABLE 18 & 35 SYSTEM
| Applicant | MicroVention, Inc., Tistin CA, US |
| Decision | Substantially Equivalent, Jun 17, 2013 |
| Received | Mar 5, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K130577
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.