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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