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3M RED DOT RESTING EKG ELECTRODE, CATALOG 2360

K974445 Class II Traditional
Decision Date
1998-07-26
Sponsor / Applicant
3M Healthcare

Technical Specification

510(k) Submission ID K974445
Product Code DRX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2360
Decision Date 1998-07-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

3M RED DOT RESTING EKG ELECTRODE, CATALOG 2360 received FDA 510(k) clearance under submission number K974445, sponsored by 3M Healthcare. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1998-07-26.

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.