K-number	K050755
Device name	MODIFICATION TO BVBLUE
Applicant	Gryphus Diagnostics, LLC
Product code	MXB
Device class	Class I
Decision date	Apr 6, 2005
Decision	Substantially Equivalent
Regulation	866.2660

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO BVBLUE

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