510(k) K171845 ยท KRD Device, Vascular, For Promoting Embolization
EMBA Hourglass Peripheral Embolization Device
| Applicant | Emba Medical Limited, Miami FL, US |
| Decision | Substantially Equivalent, Aug 18, 2017 |
| Received | Jun 20, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171845
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.