510(k) K812168 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
CORDIS DUCOR PERCUT. TRANS. ANGIO. CATH.
| Applicant | Cordis Corp., Walker MI, US |
| Decision | Substantially Equivalent, Aug 31, 1981 |
| Received | Jul 30, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K812168
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.