K-number	K130528
Device name	BIOPLEX 2200 APLS IGM
Applicant	Bio-Rad Laboratories
Product code	MID
Device class	Class II
Decision date	Oct 21, 2013
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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BIOPLEX 2200 APLS IGM

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