FDA 510(k), K142743, AliveCor Heart Monitor

FDA 510(k), K142743, AliveCor Heart Monitor

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510(K) Number: K142743
Device Name: AliveCor Heart Monitor
Manufacturer: AliveCor, Inc.
Device Classification Name: transmitters and receivers, electrocardiograph, telephone
Regulation Number: 870.2920
Classification Product Code: DXH
Date Received: 09/24/2014
Decision Date: 01/27/2015
Regulation Medical Specialty: Cardiovascular

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