K-number	K120572
Device name	BIOPLEX 2200 TORC IGG
Applicant	Bio-Rad Laboratories, Inc.
Product code	OMI
Device class	Class II
Decision date	Mar 26, 2012
Decision	Substantially Equivalent
Regulation	866.3510

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View the full FDA submission: accessdata.fda.gov

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BIOPLEX 2200 TORC IGG

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