K-number	K902393
Device name	COACUTE ANTITHROMBIN CHROMOGENIC ASSAY
Applicant	Kabi Diagnostica
Product code	JBQ
Device class	Class II
Decision date	Sep 25, 1990
Decision	Substantially Equivalent
Regulation	864.7060

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View the full FDA submission: accessdata.fda.gov

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COACUTE ANTITHROMBIN CHROMOGENIC ASSAY

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