510(k) K905297 ยท DQO Catheter, Intravascular, Diagnostic
DIAVENTIONAL CATHETER
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Feb 1, 1991 |
| Received | Nov 27, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K905297
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.