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TRANSTELEPHONIC ECG RECORDER/TRANSMITTER & RECEIVE

K854013 Class II Traditional
Decision Date
1986-02-28
Sponsor / Applicant
Medrand, Inc.

Technical Specification

510(k) Submission ID K854013
Product Code DXH
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2920
Decision Date 1986-02-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRANSTELEPHONIC ECG RECORDER/TRANSMITTER & RECEIVE received FDA 510(k) clearance under submission number K854013, sponsored by Medrand, 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 1986-02-28.

Classification & Regulation

This clearance is catalogued under FDA product code DXH and 21 CFR 870.2920, within the Cardiovascular review panel as a Class II device.