510(k) K772230 ยท LKF Cannula, Manipulator/Injector, Uterine
CANNULA, PERFUSION, FALLOPIAN TUBE
| Applicant | J. Sklar Mfg. Co., Inc., Walker MI, US |
| Decision | Substantially Equivalent, Jan 3, 1978 |
| Received | Dec 6, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K772230
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.