510(k) K182390 ยท KRD Device, Vascular, For Promoting Embolization
IMPEDE-FX Embolization Plug
| Applicant | Shape Memory Medical, Santa Clara CA, US |
| Decision | Substantially Equivalent, May 23, 2019 |
| Received | Sep 4, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182390
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.