K-number	K091616
Device name	BIOPLEX 2200 MMRV IGG
Applicant	Bio-Rad Laboratories
Product code	OPL
Device class	Class II
Decision date	Mar 29, 2010
Decision	Substantially Equivalent
Regulation	866.3510

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View the full FDA submission: accessdata.fda.gov

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BIOPLEX 2200 MMRV IGG

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