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FDA 510(k) Applications Submitted by BRAEMAR, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K071011
04/10/2007
MODIFICATION TO: BRAEMAR ER900 SERIES ENHANCED ALGORITHM ECG EVENT RECORDER
BRAEMAR, INC.
K081444
05/22/2008
BRAEMAR FUSION WIRELESS - AMBULATORY ECG ARRHYTHMIA MONITORING SYSTEM
BRAEMAR, INC.
K071733
06/26/2007
DL900 SERIES HOLTER RECORDER
BRAEMAR, INC.
K072008
07/23/2007
BRAEMAR ER900 WIRELESS SERIES ARRHYTHMIA EVENT RECORDER
BRAEMAR, INC.
K042469
09/13/2004
BRAEMAR ER800 SERIES ENHANCED ALGORITHM EVENT RECORDER
BRAEMAR, INC.
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