510(k) K946052 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
POWERFLEX(TM) 5F PTA BALLOON CATHETER
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Mar 3, 1995 |
| Received | Dec 12, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K946052
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.