K-number	K140933
Device name	ALIVECOR HEART MONITOR
Applicant	AliveCor, Inc.
Product code	DXH
Device class	Class II
Decision date	Aug 15, 2014
Decision	Substantially Equivalent
Regulation	870.2920

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Source

View the full FDA submission: accessdata.fda.gov

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ALIVECOR HEART MONITOR

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