510(k) K760605 ยท GES Blade, Scalpel
LIGHTCAST II CARBIDE BLADE
| Applicant | Merck, Sharp & Dohme, Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 5, 1976 |
| Received | Sep 8, 1976 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K760605
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.