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FETAL MONITOR #FM 750

K821580 Class II Traditional
Decision Date
1982-06-25
Sponsor / Applicant
Advantage Medical Systems, Inc.

Technical Specification

510(k) Submission ID K821580
Product Code HGM
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.2740
Decision Date 1982-06-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FETAL MONITOR #FM 750 received FDA 510(k) clearance under submission number K821580, sponsored by Advantage Medical Systems, 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 1982-06-25.

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.