K-number	K133598
Device name	CARDIOHELP SYSTEM
Applicant	Maquet Cardiopulmonary, AG
Product code	DTQ
Device class	Class II
Decision date	May 21, 2014
Decision	Substantially Equivalent
Regulation	870.4220

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Source

View the full FDA submission: accessdata.fda.gov

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CARDIOHELP SYSTEM

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