K-number	K853696
Device name	RUBELLA IGG EIA TEST KIT
Applicant	Labsystems, Inc.
Product code	LFX
Device class	Class II
Decision date	Jun 17, 1986
Decision	Substantially Equivalent
Regulation	866.3510

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View the full FDA submission: accessdata.fda.gov

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RUBELLA IGG EIA TEST KIT

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