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CT 200 ELECTROCARDIOGRAPH

K961798 Class II Traditional
Decision Date
1998-08-05
Sponsor / Applicant
Macquarie Medical Systems

Technical Specification

510(k) Submission ID K961798
Product Code DPS
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2340
Decision Date 1998-08-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CT 200 ELECTROCARDIOGRAPH received FDA 510(k) clearance under submission number K961798, sponsored by Macquarie Medical Systems. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1998-08-05.

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.