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PREGELLED INFANT DISPOSABLE ECG ELECTRODE

K862756 Class II Traditional
Decision Date
1986-08-06
Sponsor / Applicant
Labeltape Meditect, Inc.

Technical Specification

510(k) Submission ID K862756
Product Code DXN
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1130
Decision Date 1986-08-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PREGELLED INFANT DISPOSABLE ECG ELECTRODE received FDA 510(k) clearance under submission number K862756, 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 1986-08-06.

Classification & Regulation

This clearance is catalogued under FDA product code DXN and 21 CFR 870.1130, within the Cardiovascular review panel as a Class II device.