K-number	K011545
Device name	VERDICT -II TCA, VERDICT-II MTD
Applicant	Medtox Diagnostics, Inc.
Product code	LFG
Device class	Class II
Decision date	Jun 8, 2001
Decision	Substantially Equivalent
Regulation	862.3910

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View the full FDA submission: accessdata.fda.gov

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VERDICT -II TCA, VERDICT-II MTD

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