K-number	K934891
Device name	AMPHETAMINES EIA ASSAY MODIFICATION
Applicant	Diagnostic Reagents, Inc.
Product code	DKZ
Device class	Class II
Decision date	Jan 13, 1994
Decision	Substantially Equivalent
Regulation	862.3100

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View the full FDA submission: accessdata.fda.gov

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AMPHETAMINES EIA ASSAY MODIFICATION

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