510(k) K943448 ยท LKF Cannula, Manipulator/Injector, Uterine
LUMIN
| Applicant | Utah Medical Products, Inc., Midvale UT, US |
| Decision | Substantially Equivalent, Apr 11, 1995 |
| Received | Jul 18, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K943448
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.