K-number	K010668
Device name	BAYER DIAGNOSTICS ADVIA CENTAUR RUBELLA IGM ASSAY
Applicant	Bayer Corp.
Product code	LFX
Device class	Class II
Decision date	Jul 5, 2001
Decision	Substantially Equivalent
Regulation	866.3510

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BAYER DIAGNOSTICS ADVIA CENTAUR RUBELLA IGM ASSAY

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