K-number	K131497
Device name	MCKESSON CARDIOLOGY HEMO
Applicant	Mckesson Israel , Ltd.
Product code	MWI
Device class	Class II
Decision date	Dec 5, 2013
Decision	Substantially Equivalent
Regulation	870.2300

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View the full FDA submission: accessdata.fda.gov

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MCKESSON CARDIOLOGY HEMO

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