K-number	K130516
Device name	CARDIODAY
Applicant	Getemed Medizin- Und Informationstechnik AG
Product code	DQK
Device class	Class II
Decision date	Aug 23, 2013
Decision	Substantially Equivalent
Regulation	870.1425

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View the full FDA submission: accessdata.fda.gov

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CARDIODAY

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