K-number	K090147
Device name	BLOOD MONITORING UNIT, MODEL BMU 40
Applicant	Maquet Cardiopulmonary, AG
Product code	DRY
Device class	Class II
Decision date	Apr 22, 2009
Decision	Substantially Equivalent
Regulation	870.4330

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Source

View the full FDA submission: accessdata.fda.gov

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BLOOD MONITORING UNIT, MODEL BMU 40

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