510(k) K933236 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
CORDIS OPTA 5(TM), MODIFICATION
| Applicant | Cordis Corp., Miami FL, US |
| Decision | Substantially Equivalent, Dec 27, 1993 |
| Received | Jun 3, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933236
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.