FDA 510(k), K160064, MoMe Kardia Wireless Ambulatory ECG Monitoring and Detection System

FDA 510(k), K160064, MoMe Kardia Wireless Ambulatory ECG Monitoring and Detection System

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510(K) Number: K160064
Device Name: MoMe Kardia Wireless Ambulatory ECG Monitoring and Detection System
Manufacturer: NANCY BRIEFS
Device Classification Name: Outpatient Cardiac Telemetry
Regulation Number: QYX
Classification Product Code: 01/13/2016
Date Received: 03/11/2016
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
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