510(k) K962759 ยท DQO Catheter, Intravascular, Diagnostic
4F NYLEX ANGIOGRAPHIC CATHETER
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Oct 10, 1996 |
| Received | Jul 16, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962759
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.