510(k) K060078 ยท KRD Device, Vascular, For Promoting Embolization
FIBERED IDC OCCLUSION SYSTEM
| Applicant | Boston Scientific Corporation, Marlborough MA, US |
| Decision | Substantially Equivalent, Jan 31, 2006 |
| Received | Jan 10, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K060078
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.