510(k) K063563 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
CORDIS AMILA PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) BALLOON DILATATION CATHETER
| Applicant | Cordis Europa, N.V., Warren NJ, US |
| Decision | Substantially Equivalent, Mar 7, 2007 |
| Received | Nov 28, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K063563
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.