FDA 510(k) Applications Submitted by PAUL G STAPLETON

FDA 510(k) Number	Submission Date	Device Name	Applicant
K990422	02/11/1999	RENU MULTIPLUS MULTI-PURPOSE SOLUTION	BAUSCH & LOMB, INC.
K020802	03/12/2002	RENUT MULTIPLUS MULLTI-PURPOSE SOLUTION	BAUSCH & LOMB INCORPORATED
K001539	05/17/2000	RENU MULTIPLUS MULTI-PURPOSE SOLUTION	BAUSCH & LOMB, INC.
K031646	05/28/2003	BAUSCH & LOMB MULTI-PURPOSE SOLUTION NRC03	BAUSCH & LOMB, INC.
K011796	06/08/2001	RENU MULTIPLUS NO RUB MULTI-PURPOSE SOLUTION	BAUSCH & LOMB, INC.
K982775	08/07/1998	BAUSCH & LOMB RENU MULTI-PURPOSE SOLUTION	BAUSCH & LOMB, INC.
K002823	09/11/2000	RENU MULTIPLUS MULTI-PURPOSE DISINFECTING SOLUTION	BAUSCH & LOMB, INC.
K973921	10/15/1997	BAUSCH & LOMB2 SENSITIVE EYES MULTI-PURPOSE SOLUTION	BAUSCH & LOMB, INC.
K974723	12/18/1997	RENU MULTIPLUS MULTI-PURPOSE SOLUTION	BAUSCH & LOMB, INC.