K252260
- 510(k) number
- K252260
- Device name
- RELIEEV HSG Catheter (HSG7FA1)
- Applicant
- Li Medical Corporation , Ltd. TW
- Product code
- LKF — Cannula, Manipulator/Injector, Uterine
- Decision date
- 2025-11-26
- Date received
- 2025-07-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Obstetrics/Gynecology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K252260.pdf
Official FDA record: K252260
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.