510(k) K760944 ยท DQX Wire, Guide, Catheter
ANGIOGRAPHIC GUIDEWIRE
| Applicant | Medrad, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 10, 1976 |
| Received | Nov 1, 1976 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K760944
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.