K-number	K012164
Device name	'RAPIDONE'-METHADONE TEST
Applicant	American Bio Medica Corp.
Product code	DJR
Device class	Class II
Decision date	Nov 20, 2001
Decision	Substantially Equivalent
Regulation	862.3620

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View the full FDA submission: accessdata.fda.gov

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'RAPIDONE'-METHADONE TEST

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