meddevicedb.com FDA Device Reference

MULTICHANNEL TELEMETRY SYSTEM

K801944 Class II Traditional
Decision Date
1980-10-23
Sponsor / Applicant
Burdick Corp.

Technical Specification

510(k) Submission ID K801944
Product Code DRG
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2910
Decision Date 1980-10-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MULTICHANNEL TELEMETRY SYSTEM received FDA 510(k) clearance under submission number K801944, sponsored by Burdick Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1980-10-23.

Classification & Regulation

This clearance is catalogued under FDA product code DRG and 21 CFR 870.2910, within the Cardiovascular review panel as a Class II device.