K-number	K923578
Device name	LIQUICHEK RHEUMATOID FACTOR CONTROL
Applicant	Bio-Rad
Product code	DHR
Device class	Class II
Decision date	Oct 6, 1992
Decision	Substantially Equivalent
Regulation	866.5775

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View the full FDA submission: accessdata.fda.gov

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LIQUICHEK RHEUMATOID FACTOR CONTROL

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