K-number	K081444
Device name	BRAEMAR FUSION WIRELESS - AMBULATORY ECG ARRHYTHMIA MONITORING SYSTEM
Applicant	Braemar, Inc.
Product code	DSI
Device class	Class II
Decision date	Jul 31, 2008
Decision	Substantially Equivalent
Regulation	870.1025

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View the full FDA submission: accessdata.fda.gov

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BRAEMAR FUSION WIRELESS - AMBULATORY ECG ARRHYTHMIA MONITORING SYSTEM

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