510(k) K894899 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
EXPANSION OF THE CORDIS PTA DILATATION CATHETER
| Applicant | Cordis Corp., Miami FL, US |
| Decision | Substantially Equivalent, Jan 26, 1990 |
| Received | Aug 1, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894899
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.