K-number	K041743
Device name	ACON TRI-FECT DRUG SCREEN TEST DEVICE
Applicant	ACON Laboratories, Inc.
Product code	DKZ
Device class	Class II
Decision date	Sep 9, 2004
Decision	Substantially Equivalent
Regulation	862.3100

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Source

View the full FDA submission: accessdata.fda.gov

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ACON TRI-FECT DRUG SCREEN TEST DEVICE

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