510(k) K872248 ยท DQO Catheter, Intravascular, Diagnostic
DOUBLE LUMEN CATHETER
| Applicant | Cordis Corp., Miami FL, US |
| Decision | Substantially Equivalent, Aug 12, 1987 |
| Received | Jun 12, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K872248
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.