K-number	K162023
Device name	CardioDay V2.5
Applicant	Getemed Medizin- Und Informationstechnik AG
Product code	DQK
Device class	Class II
Decision date	Mar 24, 2017
Decision	Substantially Equivalent
Regulation	870.1425

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Source

View the full FDA submission: accessdata.fda.gov

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CardioDay V2.5

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