K-number	K122272
Device name	CARDIOMEM
Applicant	Getemed Medizin- Und Informationstechnik AG
Product code	MWJ
Device class	Class II
Decision date	Mar 28, 2013
Decision	Substantially Equivalent
Regulation	870.2800

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View the full FDA submission: accessdata.fda.gov

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CARDIOMEM

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