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RESUBMITTED STANDARD MICROPORE ECG ELECTRODE

K874628 Class II Traditional
Decision Date
1987-12-07
Sponsor / Applicant
Labeltape Meditect, Inc.

Technical Specification

510(k) Submission ID K874628
Product Code DRX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2360
Decision Date 1987-12-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RESUBMITTED STANDARD MICROPORE ECG ELECTRODE received FDA 510(k) clearance under submission number K874628, sponsored by Labeltape Meditect, 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 1987-12-07.

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.