Clearance Summary
KEGELMASTER 2000 received FDA 510(k) clearance under submission number K023305, sponsored by Kegelmaster 2000 , Ltd.. 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 2002-12-26.
- Submission: K023305
- Applicant / Sponsor: Kegelmaster 2000 , Ltd.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.1425
- Decision date: 2002-12-26
Classification & Regulation
This clearance is catalogued under FDA product code HIR and 21 CFR 884.1425, within the Obstetrics/Gynecology review panel as a Class II device.