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FDA 510(k) Applications Submitted by DAVID NORBERG
FDA 510(k) Number
Submission Date
Device Name
Applicant
K030856
03/18/2003
ER800 SERIES ECG EVENT RECORDER
BRAEMAR CORP.
K981394
04/17/1998
BRAEMAR ER700 SERIES AMBULATORY ECG EVENT MONITOR MODELS ER710,ER720
BRAEMAR CORP.
K993617
10/26/1999
DIGITRAKPLUS HOLTER RECORDER
BRAEMAR CORP.
K993618
10/26/1999
DXP1000 HOLTER RECORDER
BRAEMAR CORP.
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