510(k) K915374 ยท DQY Catheter, Percutaneous
CORDIS 6 FRENCH 0.062 I.D. PTCA GUIDING CATHTER
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Feb 14, 1992 |
| Received | Nov 29, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K915374
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.