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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