Clearance Summary
KEVOR-CURETTE received FDA 510(k) clearance under submission number K882404, sponsored by Euro-Med Intl.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 1988-07-08.
- Submission: K882404
- Applicant / Sponsor: Euro-Med Intl.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.1050
- Decision date: 1988-07-08
Classification & Regulation
This clearance is catalogued under FDA product code PCF and 21 CFR 884.1050, within the Obstetrics/Gynecology review panel as a Class II device.