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ADDITIONAL USE FOR ECG DISPOSABLE ELECTRODE V-PAD

K864690 Class II Traditional
Decision Date
1987-05-06
Sponsor / Applicant
Multi Biosensors, Inc.

Technical Specification

510(k) Submission ID K864690
Product Code DRX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2360
Decision Date 1987-05-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ADDITIONAL USE FOR ECG DISPOSABLE ELECTRODE V-PAD received FDA 510(k) clearance under submission number K864690, sponsored by Multi Biosensors, 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 1987-05-06.

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.