K-number	K103801
Device name	HYPOTHERMX INTRAVENOUS FLUID WARMER
Applicant	Emit Corporation
Product code	LGZ
Device class	Class II
Decision date	May 20, 2011
Decision	Substantially Equivalent
Regulation	880.5725

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View the full FDA submission: accessdata.fda.gov

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HYPOTHERMX INTRAVENOUS FLUID WARMER

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