Clearance Summary
FETASCAN 2000,2000A OBSTETRICAL DATA received FDA 510(k) clearance under submission number K813457, sponsored by Cranbury Medical Labs, 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 1982-02-12.
- Submission: K813457
- Applicant / Sponsor: Cranbury Medical Labs, Inc.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.2740
- Decision date: 1982-02-12
Classification & Regulation
This clearance is catalogued under FDA product code HGM and 21 CFR 884.2740, within the Obstetrics/Gynecology review panel as a Class II device.