K-number	K990681
Device name	DBSET MULTIDRUG SCREEN TEST KIT
Applicant	Ameritek, Inc.
Product code	DKZ
Device class	Class II
Decision date	Jul 15, 1999
Decision	Substantially Equivalent
Regulation	862.3100

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View the full FDA submission: accessdata.fda.gov

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DBSET MULTIDRUG SCREEN TEST KIT

Everything you need for a 510(k) submission. Nothing you don't.