Clearance Summary
UTERINE MANIPULATOR/INJECTOR received FDA 510(k) clearance under submission number K974357, sponsored by Catheter Research, 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 1998-02-02.
- Submission: K974357
- Applicant / Sponsor: Catheter Research, Inc.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.4530
- Decision date: 1998-02-02
Classification & Regulation
This clearance is catalogued under FDA product code LKF and 21 CFR 884.4530, within the Obstetrics/Gynecology review panel as a Class II device.