K-number	K993482
Device name	K-ASSAY FIBRINOGEN
Applicant	Kamiya Biomedical Co.
Product code	GIS
Device class	Class II
Decision date	Dec 6, 1999
Decision	Substantially Equivalent
Regulation	864.7340

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View the full FDA submission: accessdata.fda.gov

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K-ASSAY FIBRINOGEN

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