K-number	K102342
Device name	KEYPATH(TM) MRSA/MSSA BLOOD CULTURE TEST- BT
Applicant	Microphage, Inc.
Product code	OUS
Device class	Class I
Decision date	May 5, 2011
Decision	Substantially Equivalent
Regulation	866.2050

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View the full FDA submission: accessdata.fda.gov

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KEYPATH(TM) MRSA/MSSA BLOOD CULTURE TEST- BT

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