K-number	K894573
Device name	SCANLISA HUMAN CRP ELISA KIT
Applicant	Immuntech A/S
Product code	DCK
Device class	Class II
Decision date	Aug 10, 1989
Decision	Substantially Equivalent
Regulation	866.5270

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View the full FDA submission: accessdata.fda.gov

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SCANLISA HUMAN CRP ELISA KIT

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