K240434
- 510(k) number
- K240434
- Device name
- RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6)
- Applicant
- Li Medical Corporation , Ltd. TW
- Product code
- HHK — Curette, Suction, Endometrial (And Accessories)
- Decision date
- 2024-09-25
- Date received
- 2024-02-14
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Obstetrics/Gynecology
510(k) Summary (official FDA PDF): K240434.pdf
Official FDA record: K240434
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.