FDA 510(k), K152491, MoMe Software Platform

FDA 510(k), K152491, MoMe Software Platform

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510(K) Number: K152491
Device Name: MoMe Software Platform
Manufacturer:
Device Classification Name: Detector And Alarm, Arrhythmia
Regulation Number: 870.1025
Classification Product Code: DSI
Date Received: 09/01/2015
Decision Date: 12/17/2015
Regulation Medical Specialty: Cardiovascular
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