K-number	K123288
Device name	HEMOCONCENTRATOR
Applicant	Maquet Cardiopulmonary, AG
Product code	KDI
Device class	Class II
Decision date	Jun 26, 2013
Decision	Substantially Equivalent
Regulation	876.5860

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Source

View the full FDA submission: accessdata.fda.gov

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HEMOCONCENTRATOR

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