K-number	K910592
Device name	ABUSCREEN FP FOR CANNABINOIDS (15-50)
Applicant	Roche Diagnostic Systems, Inc.
Product code	LDJ
Device class	Class II
Decision date	Jun 21, 1991
Decision	Substantially Equivalent
Regulation	862.3870

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View the full FDA submission: accessdata.fda.gov

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ABUSCREEN FP FOR CANNABINOIDS (15-50)

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