510(k) K093681 ยท DQX Wire, Guide, Catheter
MERIDIAN GUIDEWIRE
| Applicant | Ev3 Neurovascular, Irvine CA, US |
| Decision | Substantially Equivalent, Jan 26, 2010 |
| Received | Nov 27, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093681
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.