510(k) K123696 ยท KRD Device, Vascular, For Promoting Embolization
MEDUSA VASCULAR PLUG
| Applicant | Endoshape, Inc., Boulder CO, US |
| Decision | Substantially Equivalent, Oct 25, 2013 |
| Received | Dec 3, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123696
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.