K-number	K962523
Device name	N LATEX CRP MONO REAGENT
Applicant	Behring Diagnostics, Inc.
Product code	DCK
Device class	Class II
Decision date	Jul 10, 1996
Decision	Substantially Equivalent
Regulation	866.5270

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View the full FDA submission: accessdata.fda.gov

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N LATEX CRP MONO REAGENT

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