510(k) K832698 ยท LYK Angioscope
ANGIOSCOPY CATHETER
| Applicant | American Edwards Laboratories, Walker MI, US |
| Decision | Substantially Equivalent, Nov 3, 1983 |
| Received | Aug 10, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832698
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.