510(k) K003920 ยท DQY Catheter, Percutaneous
CORDIS M3 PTA DILATATION CATHETER
| Applicant | Cordis Corp., Warren NJ, US |
| Decision | Substantially Equivalent, Jun 15, 2001 |
| Received | Dec 19, 2000 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K003920
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.