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TAYLOR LONG TERM MONITORING ELECTRODE

K941977 Class II Traditional
Decision Date
1994-09-21
Sponsor / Applicant
Taylor Industries, Inc.

Technical Specification

510(k) Submission ID K941977
Product Code DRX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2360
Decision Date 1994-09-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TAYLOR LONG TERM MONITORING ELECTRODE received FDA 510(k) clearance under submission number K941977, sponsored by Taylor Industries, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1994-09-21.

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.