RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6)— 510(k) K240434
Substantially EquivalentLi Medical Corporation , Ltd.
FDA 510(k) clearance K240434 for RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6), Substantially Equivalent on 2024-09-25. Applicant: Li Medical Corporation , Ltd..
Clearance details
- Applicant
- Li Medical Corporation , Ltd.
- Product code
- Code HHK
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- New Taipei City, TW
Data sourced from openFDA. This site is unofficial and independent of the FDA.