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LIFE TRACE FETAL SPIRAL ELECTRODE WITH MATERNAL REFERENCE

K943732 Class II Traditional
Decision Date
1994-10-20
Sponsor / Applicant
Graphic Controls Corp.

Technical Specification

510(k) Submission ID K943732
Product Code HGP
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.2675
Decision Date 1994-10-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LIFE TRACE FETAL SPIRAL ELECTRODE WITH MATERNAL REFERENCE received FDA 510(k) clearance under submission number K943732, sponsored by Graphic Controls Corp.. 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 1994-10-20.

Classification & Regulation

This clearance is catalogued under FDA product code HGP and 21 CFR 884.2675, within the Obstetrics/Gynecology review panel as a Class II device.