K-number	K924056
Device name	ENCORE RHEUMATOID FACTOR EIA
Applicant	Clark Laboratories, Inc.
Product code	DHR
Device class	Class II
Decision date	Sep 25, 1992
Decision	Substantially Equivalent
Regulation	866.5775

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View the full FDA submission: accessdata.fda.gov

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ENCORE RHEUMATOID FACTOR EIA

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