K-number	K980872
Device name	RAPID DRUG SCREEN' 8 PANEL
Applicant	American Bio Medica Corp.
Product code	DIO
Device class	Class II
Decision date	Mar 20, 1998
Decision	Substantially Equivalent
Regulation	862.3250

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View the full FDA submission: accessdata.fda.gov

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RAPID DRUG SCREEN' 8 PANEL

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