K-number	K914028
Device name	RUBELLA IGM ELISA TEST SYSTEM
Applicant	Zeus Scientific, Inc.
Product code	LFX
Device class	Class II
Decision date	Apr 22, 1992
Decision	Substantially Equivalent
Regulation	866.3510

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View the full FDA submission: accessdata.fda.gov

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RUBELLA IGM ELISA TEST SYSTEM

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