K-number	K890399
Device name	MODIFIED D-DI-TEST KIT
Applicant	American Bioproducts Co.
Product code	GHH
Device class	Class II
Decision date	Feb 7, 1989
Decision	Substantially Equivalent
Regulation	864.7320

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View the full FDA submission: accessdata.fda.gov

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MODIFIED D-DI-TEST KIT

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