510(k) K930479 ยท DQO Catheter, Intravascular, Diagnostic
NYLEX CATHETERS
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Apr 21, 1993 |
| Received | Jan 29, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930479
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.