510(k) K133208 ยท KRD Device, Vascular, For Promoting Embolization
INTERLOCK-35 FIBERED IDC OCCLUSION SYSTEM
| Applicant | Boston Scientific Corp, Maple Grove MN, US |
| Decision | Substantially Equivalent, Nov 14, 2013 |
| Received | Oct 18, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K133208
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.