K-number	K013637
Device name	ACTICHROME HEPARIN (ANTI-FIIA)
Applicant	American Diagnostica, Inc.
Product code	KFF
Device class	Class II
Decision date	Apr 16, 2002
Decision	Substantially Equivalent
Regulation	864.7525

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View the full FDA submission: accessdata.fda.gov

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ACTICHROME HEPARIN (ANTI-FIIA)

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