510(k) K240364 ยท LKF Cannula, Manipulator/Injector, Uterine
RELIEEV Uterine Manipulator Injector (CUMI 5.0)
| Applicant | Li Medical Corporation , Ltd., Xizhi Dist., TW |
| Decision | Substantially Equivalent, Oct 16, 2024 |
| Received | Feb 6, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240364
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.