K-number	K821804
Device name	RUBELLA RQ BIO-ENZABEAD KIT
Applicant	Litton Bionetics
Product code	LFX
Device class	Class II
Decision date	Sep 14, 1982
Decision	Substantially Equivalent
Regulation	866.3510

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View the full FDA submission: accessdata.fda.gov

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RUBELLA RQ BIO-ENZABEAD KIT

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