510(k) K003159 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
CORDIS SLALOM PTA BALLOON CATHETER
| Applicant | Cordis Corp., Warren NJ, US |
| Decision | Substantially Equivalent, Oct 30, 2000 |
| Received | Oct 10, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K003159
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.