510(k) K932432 ยท LKF Cannula, Manipulator/Injector, Uterine
KRONNER REINFORCING STYLETTE
| Applicant | Unimar, Inc., Wilton CT, US |
| Decision | Substantially Equivalent, Apr 12, 1994 |
| Received | May 20, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932432
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.