510(k) K931814 ยท LKF Cannula, Manipulator/Injector, Uterine
DMI UTERINE MOBILIZER/ELEVATOR/CANNULA
| Applicant | Diversified Medical Instruments, Inc., Ellicott City MD, US |
| Decision | Substantially Equivalent, May 31, 1994 |
| Received | Apr 8, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K931814
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.