510(k) K252260 ยท LKF Cannula, Manipulator/Injector, Uterine
RELIEEV HSG Catheter (HSG7FA1)
| Applicant | Li Medical Corporation , Ltd., Xizhi Dist., TW |
| Decision | Substantially Equivalent, Nov 26, 2025 |
| Received | Jul 21, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K252260
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.