510(k) K834220 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
HYBRID PERIPHERAL DILATION CATHETER
| Applicant | American Edwards Laboratories, Walker MI, US |
| Decision | Substantially Equivalent, Jan 27, 1984 |
| Received | Dec 5, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K834220
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.