510(k) K213398 ยท KRD Device, Vascular, For Promoting Embolization
EMBOLD Fibered Detachable Coil System
| Applicant | Boston Scientific Corporation, Maple Grove MN, US |
| Decision | Substantially Equivalent, Apr 12, 2022 |
| Received | Oct 18, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K213398
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.