510(k) K991673 ยท DQO Catheter, Intravascular, Diagnostic
CORDIS TEMPO ANGIOGRAPHY CATHETER
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, May 26, 1999 |
| Received | May 17, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K991673
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.