K-number	K011609
Device name	LIVESURE AMPHETAMINE SCREEN TEST
Applicant	Pan Probe Biotech, Inc.
Product code	DKZ
Device class	Class II
Decision date	Jun 8, 2001
Decision	Substantially Equivalent
Regulation	862.3100

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Source

View the full FDA submission: accessdata.fda.gov

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LIVESURE AMPHETAMINE SCREEN TEST

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