FDA 510(k) Applications Submitted by NEIL ANDERSON

FDA 510(k) Number	Submission Date	Device Name	Applicant
K980174	01/20/1998	DUREX COLORS AND SCENTS	LONDON INTL. LLC.
K980204	01/20/1998	DUREX LATEX CONDOMS	LONDON INTL. LLC.
K160234	02/01/2016	OVENT	OVENTUS MANUFACTURING PTY LTD
K960590	02/12/1996	TRI-CLEAN 110/TRI-CLEAN PLUS GLOVE	ALADAN CORP.
K980785	03/02/1998	STERILE, POWDERFREE LATEX EXAMINATION GLOVE	LONDON INTL. LLC.
K080606	03/04/2008	ALATECH POWDERED LATEX PATIENT EXAMINATION GLOVE	ALATECH HEALTHCARE, LLC.
K970924	03/07/1997	REGENT BIOGEL SURGICAL GLOVE, BIOGEL M GLOVE	REGENT MEDICAL
K980942	03/12/1998	REGENT BIOGEL INDICATOR INNER SURGICAL GLOVE	LONDON INTERNATIONAL GROUP, INC.
K971514	04/25/1997	REGENT BIOGEL DIAGNOSTIC PROCEDURE GLOVE	LONDON INTERNATIONAL GROUP, INC.
K982924	08/20/1998	DUREX SENSIDOM LATEX CONDOM	LONDON INTL. LLC.
K082529	09/02/2008	ALATECH CHAMPION VYTEX LUBRICATED MALE LATEX CONDOM	ALATECH HEALTHCARE, LLC.
K983380	09/25/1998	DUREX LUBRAGEL LATEX CONDOM	LONDON INTL. LLC.
K984249	11/30/1998	SKINSENSE NITRILE POWDER-FREE SYNTHETIC MEDICAL EXAMINATION GLOVE	LONDON INTERNATIONAL GROUP, INC.
K083761	12/18/2008	ALATECH POWDER FREE LATEX EXAMINATION GLOVE	ALATECH HEALTHCARE, LLC.
K980319	01/27/1998	DUREX ULTRA COMFORT	LONDON INTL. LLC.
K980516	02/10/1998	REGENT BIOGEL ORTHOPEDIC SURGICAL GLOVE	LONDON INTERNATIONAL GROUP, INC.