510(k) K803057 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
FOGARTY BALLON ANGIOPLASTY CATHETERS
| Applicant | American Edwards Laboratories, Walker MI, US |
| Decision | Substantially Equivalent, Jan 13, 1981 |
| Received | Dec 2, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K803057
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.