Clearance Summary
BABY DOPPLEX 4000, MODEL BD 4000 received FDA 510(k) clearance under submission number K990569, sponsored by Huntleigh Healthcare, 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 2000-01-24.
- Submission: K990569
- Applicant / Sponsor: Huntleigh Healthcare, Inc.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.2740
- Decision date: 2000-01-24
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.