510(k) K032737 ยท DQY Catheter, Percutaneous
CORDIS POWERFLEX EXTREME PTA BALLOON CATHETER, CORDIS POWERFLEX PLUS PTA BALLOON CATHETER, CORDIS POWERFLEX P3 PTA
| Applicant | Cordis Europa, N.V., Warren NJ, US |
| Decision | Substantially Equivalent, Oct 2, 2003 |
| Received | Sep 4, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K032737
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Feb 28, 2020 | Cordis Corporation Cordis POWERFLEX P3, PTA Dilation Catheter, REF 420-6020S Terminated |
LIT | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.