510(k) K932394 ยท LKF Cannula, Manipulator/Injector, Uterine
BERNSTEIN(TM) UTERINE MANIPULATOR
| Applicant | Gm Engineering, Inc., La Verne CA, US |
| Decision | Substantially Equivalent, Jan 26, 1995 |
| Received | May 18, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932394
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.