510(k) K151676 ยท KRD Device, Vascular, For Promoting Embolization
Retracta Detachable Embolization Coil
| Applicant | Cook Incorporated, Bloomington IN, US |
| Decision | Substantially Equivalent, Jul 22, 2015 |
| Received | Jun 22, 2015 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K151676
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.