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FDA 510(k) Applications Submitted by DONNA-BEA TILLMAN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K130401
02/19/2013
ALERTWATCH: OR
ALERTWATCH LLC
DEN180042
08/09/2018
Irregular Rhythm Notification Feature
Apple Inc
DEN180044
08/14/2018
ECG App
Apple Inc
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