K-number	K011011
Device name	LIVESURE MORPHINE SCREEN TEST
Applicant	Pan Probe Biotech, Inc.
Product code	DOE
Device class	Class II
Decision date	Apr 13, 2001
Decision	Substantially Equivalent
Regulation	862.3640

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View the full FDA submission: accessdata.fda.gov

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LIVESURE MORPHINE SCREEN TEST

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