FDA 510(k) Applications Submitted by JOHN B DUBECK

FDA 510(k) Number	Submission Date	Device Name	Applicant
K980872	03/06/1998	RAPID DRUG SCREEN' 8 PANEL	AMERICAN BIO MEDICA CORP.
K990818	03/11/1999	RAPIDONE - MARIJUANA TEST	AMERICAN BIO MEDICA CORP.
K990820	03/11/1999	RAPIDONE - OPIATES TEST	AMERICAN BIO MEDICA CORP.
K990822	03/11/1999	RAPIDONE - COCAINE TEST	AMERICAN BIO MEDICA CORP.
K981705	05/14/1998	'RAPID DRUG SCREEN' 8 PANEL-LOW VOLUME	AMERICAN BIO MEDICA CORP.
K992033	06/16/1999	MODIFICATION TO 'RAPID DRUG SCREEN' 9-PANEL	AMERICAN BIO MEDICA CORP.
K962412	06/21/1996	NIKE V8 AND NIKE V12	NIKE, INC.
K992451	07/22/1999	RAPIDONE- BARBITURATE TEST	AMERICAN BIO MEDICA CORP.
K992452	07/22/1999	RAPIDONE-AMPHETAMINE TEST	AMERICAN BIO MEDICA CORP.
K002447	08/09/2000	MODIFICATION TO RAPID DRUG SCREEN 9-PANEL	AMERICAN BIO MEDICA CORP.
K992720	08/13/1999	RAPIDONE- BENZODIAZEPINE TEST	AMERICAN BIO MEDICA CORP.
K993151	09/21/1999	RADID DRUG SCREEN 5-PANEL TEST	AMERICAN BIO MEDICA CORP.
K983770	10/26/1998	'RAPID DRUG SCREEN' 9-PANEL	AMERICAN BIO MEDICA CORP.