Clearance Summary
FEMRX MORCELLATOR SYSTEM received FDA 510(k) clearance under submission number K963872, sponsored by Gynecare Innovation Center. 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 1997-01-17.
- Submission: K963872
- Applicant / Sponsor: Gynecare Innovation Center
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.1720
- Decision date: 1997-01-17
Classification & Regulation
This clearance is catalogued under FDA product code HET and 21 CFR 884.1720, within the Obstetrics/Gynecology review panel as a Class II device.