510(k) K880612 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
CORDIS PTA DILATATION CATHETERS
| Applicant | Cordis Corp., Miami FL, US |
| Decision | Substantially Equivalent, Jul 28, 1988 |
| Received | Feb 16, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880612
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.