510(k) K992825 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
CORDIS EXTREME PTA BALLOON CATHETER
| Applicant | Cordis Corp., Warren NJ, US |
| Decision | Substantially Equivalent, Sep 15, 1999 |
| Received | Aug 23, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K992825
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.