510(k) K230706 · KRD Device, Vascular, For Promoting Embolization
EMBOLD Soft Detachable Coil System
| Applicant | Boston Scientific Corporation, Boston MA, US |
| Decision | Substantially Equivalent, Jun 27, 2023 |
| Received | Mar 14, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230706
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.