K-number	K841200
Device name	RUBELLA IGG ANTIBODY ELISA TEST SYS
Applicant	Ortho Diagnostic Systems, Inc.
Product code	LFX
Device class	Class II
Decision date	May 21, 1984
Decision	Substantially Equivalent
Regulation	866.3510

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View the full FDA submission: accessdata.fda.gov

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RUBELLA IGG ANTIBODY ELISA TEST SYS

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