510(k) K000579 ยท DQO Catheter, Intravascular, Diagnostic
TEMPO AQUA ANGIOGRAPHIC CATHETER
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, May 3, 2000 |
| Received | Feb 22, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K000579
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.