K-number	K053035
Device name	ACRO BIOTECH LLC RAPID BENZOYLECGONINE URINE TEST; CATALOG# MET001000
Applicant	Acro Biotech, LLC
Product code	DIO
Device class	Class II
Decision date	May 5, 2006
Decision	Substantially Equivalent
Regulation	862.3250

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View the full FDA submission: accessdata.fda.gov

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ACRO BIOTECH LLC RAPID BENZOYLECGONINE URINE TEST; CATALOG# MET001000

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