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PRN ECG ELECTRODE

K850130 Class II Traditional
Decision Date
1985-04-09
Sponsor / Applicant
Consolidated Medical Equipment, Inc.

Technical Specification

510(k) Submission ID K850130
Product Code DRX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2360
Decision Date 1985-04-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PRN ECG ELECTRODE received FDA 510(k) clearance under submission number K850130, sponsored by Consolidated Medical Equipment, 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 1985-04-09.

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.