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ELECTROTRACE DISP REST EKG ELECTRODE, CAT. ET1200

K871626 Class II Traditional
Decision Date
1987-06-05
Sponsor / Applicant
Jason Marketing Co.

Technical Specification

510(k) Submission ID K871626
Product Code DRX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2360
Decision Date 1987-06-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELECTROTRACE DISP REST EKG ELECTRODE, CAT. ET1200 received FDA 510(k) clearance under submission number K871626, sponsored by Jason Marketing Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1987-06-05.

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.