K-number	K072617
Device name	ELECSYS RUBELLA IGG IMMUNOASSAY
Applicant	Roche Diagnostics Corp.
Product code	LFX
Device class	Class II
Decision date	Dec 5, 2008
Decision	Substantially Equivalent
Regulation	866.3510

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View the full FDA submission: accessdata.fda.gov

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ELECSYS RUBELLA IGG IMMUNOASSAY

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