Clearance Summary
HYSTEROMAT(TM) 3700 received FDA 510(k) clearance under submission number K921871, sponsored by F.M. Wiest USA, Inc.. 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 1994-12-15.
- Submission: K921871
- Applicant / Sponsor: F.M. Wiest USA, Inc.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.1700
- Decision date: 1994-12-15
Classification & Regulation
This clearance is catalogued under FDA product code HIG and 21 CFR 884.1700, within the Obstetrics/Gynecology review panel as a Class II device.