510(k) K113651 ยท KRD Device, Vascular, For Promoting Embolization
INTERLOCK-35 FIBERED IDC OCCLUSION SYSTEM
| Applicant | Boston Scientific Corporation, Maple Grove MN, US |
| Decision | Substantially Equivalent, Jan 11, 2012 |
| Received | Dec 12, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K113651
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.