510(k) K924554 ยท LYK Angioscope
CLARUS SERIRS 2200 SEMI-RIGID ENDOSCOPE
| Applicant | Clarus Medical Systems, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Feb 25, 1993 |
| Received | Sep 9, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924554
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.