510(k) K102912 ยท KRD Device, Vascular, For Promoting Embolization
INTERLOCK FIBERED IDC OCCLUSION SYSTEM
| Applicant | Boston Scientific, Maple Grove MN, US |
| Decision | Substantially Equivalent, Mar 3, 2011 |
| Received | Oct 1, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102912
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.