K-number	K850160
Device name	FISHER DIAGNOSTICS LATEST-CRP TEST KIT
Applicant	Fisher Diagnostics
Product code	DCK
Device class	Class II
Decision date	Apr 19, 1985
Decision	Substantially Equivalent
Regulation	866.5270

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View the full FDA submission: accessdata.fda.gov

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FISHER DIAGNOSTICS LATEST-CRP TEST KIT

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