510(k) K955637 ยท DQX Wire, Guide, Catheter
ESSENCE GUIDEWIRE
| Applicant | Cordis Neurovascular, Inc., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Mar 11, 1996 |
| Received | Dec 11, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955637
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.