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BRAEMAR ER800 SERIES ENHANCED ALGORITHM EVENT RECORDER

K042469 Class II Traditional
Decision Date
2004-10-06
Sponsor / Applicant
Braemar, Inc.

Technical Specification

510(k) Submission ID K042469
Product Code MWJ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2800
Decision Date 2004-10-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BRAEMAR ER800 SERIES ENHANCED ALGORITHM EVENT RECORDER received FDA 510(k) clearance under submission number K042469, sponsored by Braemar, 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 2004-10-06.

Classification & Regulation

This clearance is catalogued under FDA product code MWJ and 21 CFR 870.2800, within the Cardiovascular review panel as a Class II device.