K-number	K122397
Device name	LIAISON RUBELLA IGM, LIAISON CONTROL RUBELLA IGM
Applicant	DiaSorin, Inc.
Product code	LFX
Device class	Class II
Decision date	Sep 6, 2012
Decision	Substantially Equivalent
Regulation	866.3510

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View the full FDA submission: accessdata.fda.gov

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LIAISON RUBELLA IGM, LIAISON CONTROL RUBELLA IGM

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