510(k) K831659 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
FOGARTY-CHIN PERIPHERAL INTRAOPERATIVE
| Applicant | American Edwards Laboratories, Walker MI, US |
| Decision | Substantially Equivalent, Aug 12, 1983 |
| Received | May 23, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831659
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.