510(k) K940868 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
CORDIS OPTA 5(TM) PTA BALLOON CATHETER, MODIFICATION
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Jul 12, 1994 |
| Received | Feb 22, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K940868
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.