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MC6700 MULTI-CHANNEL ELECTROCARDIOGRAPH

K883454 Class II Traditional
Decision Date
1989-01-25
Sponsor / Applicant
Cambridge Medical Instruments, Inc.

Technical Specification

510(k) Submission ID K883454
Product Code DPS
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2340
Decision Date 1989-01-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MC6700 MULTI-CHANNEL ELECTROCARDIOGRAPH received FDA 510(k) clearance under submission number K883454, sponsored by Cambridge Medical Instruments, 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 1989-01-25.

Classification & Regulation

This clearance is catalogued under FDA product code DPS and 21 CFR 870.2340, within the Cardiovascular review panel as a Class II device.