K-number	K960324
Device name	HEMAGEN CRP 150 KIT (EIA METHOD)
Applicant	Hemagen Diagnostics, Inc.
Product code	DCK
Device class	Class II
Decision date	Mar 12, 1996
Decision	Substantially Equivalent
Regulation	866.5270

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View the full FDA submission: accessdata.fda.gov

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HEMAGEN CRP 150 KIT (EIA METHOD)

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