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FDA 510(k) Applications Submitted by Kent Sayler
FDA 510(k) Number
Submission Date
Device Name
Applicant
K130294
02/06/2013
BRAEMAR CARDIOKEY HOLTER RECORDER
BRAEMAR MANUFACTURING LLC
K171410
05/15/2017
ePatch
Braemar Manufacturing, LLC
K093288
10/20/2009
CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION
CARDIONET, INC
K153473
12/02/2015
Braemar Telemetry Patch System
Braemar Manufacturing, LLC
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