510(k) K974357 ยท LKF Cannula, Manipulator/Injector, Uterine
UTERINE MANIPULATOR/INJECTOR
| Applicant | Catheter Research, Inc., Indianapolis IN, US |
| Decision | Substantially Equivalent, Feb 2, 1998 |
| Received | Nov 19, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K974357
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.