510(k) K971646 ยท DQO Catheter, Intravascular, Diagnostic
4F NYLEX ANGIOGRAPHY CATHETER/5F NYLEX ANGIOGRAPHY CATHETER
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Jul 14, 1997 |
| Received | May 5, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971646
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.