Clearance Summary
WALLACH CC/BRUSH received FDA 510(k) clearance under submission number K896065, sponsored by Wallach Surgical Devices, 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 1990-01-04.
- Submission: K896065
- Applicant / Sponsor: Wallach Surgical Devices, Inc.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.4530
- Decision date: 1990-01-04
Classification & Regulation
This clearance is catalogued under FDA product code HHT and 21 CFR 884.4530, within the Obstetrics/Gynecology review panel as a Class II device.