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MEDI-TRACE 5700 RESTING ECG ELECTRODE

K963151 Class II Traditional
Decision Date
1996-11-19
Sponsor / Applicant
Graphic Controls Corp.

Technical Specification

510(k) Submission ID K963151
Product Code DRX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2360
Decision Date 1996-11-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDI-TRACE 5700 RESTING ECG ELECTRODE received FDA 510(k) clearance under submission number K963151, sponsored by Graphic Controls Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1996-11-19.

Classification & Regulation

This clearance is catalogued under FDA product code DRX and 21 CFR 870.2360, within the Cardiovascular review panel as a Class II device.