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CARDIAC EVENT RECORDER (INSTANT MEMORY 2000)

K942586 Class II Traditional
Decision Date
1995-05-10
Sponsor / Applicant
Telescan Medical Systems

Technical Specification

510(k) Submission ID K942586
Product Code DXH
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2920
Decision Date 1995-05-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CARDIAC EVENT RECORDER (INSTANT MEMORY 2000) received FDA 510(k) clearance under submission number K942586, sponsored by Telescan 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 1995-05-10.

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.