510(k) K963000 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
MAXI LD PTA BALLOON CATHETER
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Feb 20, 1997 |
| Received | Aug 2, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963000
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.