K-number	K992720
Device name	RAPIDONE- BENZODIAZEPINE TEST
Applicant	American Bio Medica Corp.
Product code	JXM
Device class	Class II
Decision date	Apr 3, 2000
Decision	Substantially Equivalent
Regulation	862.3170

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View the full FDA submission: accessdata.fda.gov

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RAPIDONE- BENZODIAZEPINE TEST

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