Clearance Summary
COLPO CUP CVC-2000 received FDA 510(k) clearance under submission number K974563, sponsored by Clinical Innovations, 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 1998-03-02.
- Submission: K974563
- Applicant / Sponsor: Clinical Innovations, Inc.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.4530
- Decision date: 1998-03-02
Classification & Regulation
This clearance is catalogued under FDA product code HDP and 21 CFR 884.4530, within the Obstetrics/Gynecology review panel as a Class II device.