Clearance Summary
HUNTLEIGH FETAL DOPPLER, FD-1 & DOPCORD, D140 received FDA 510(k) clearance under submission number K900618, sponsored by Huntleigh Technology, 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 1990-04-25.
- Submission: K900618
- Applicant / Sponsor: Huntleigh Technology, Inc.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.2660
- Decision date: 1990-04-25
Classification & Regulation
This clearance is catalogued under FDA product code KNG and 21 CFR 884.2660, within the Obstetrics/Gynecology review panel as a Class II device.