K-number	K962675
Device name	STA - LIATEST VWF TEST KIT
Applicant	American Bioproducts Co.
Product code	GJT
Device class	Class II
Decision date	Oct 25, 1996
Decision	Substantially Equivalent
Regulation	864.7290

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View the full FDA submission: accessdata.fda.gov

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STA - LIATEST VWF TEST KIT

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