K-number	K911610
Device name	ELISA COMBI-KIT HUMAN IGG SUBCLASSES
Applicant	Janssen Research Foundation
Product code	DEW
Device class	Class II
Decision date	Jun 12, 1991
Decision	Substantially Equivalent
Regulation	866.5510

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View the full FDA submission: accessdata.fda.gov

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ELISA COMBI-KIT HUMAN IGG SUBCLASSES

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