FDA 510(k) Applications Submitted by OPTI-CENTRE LABORATORIES

FDA 510(k) Number	Submission Date	Device Name	Applicant
K043129	11/12/2004	PROCLEAR ULTRAVUE MULTIFOCAL AND PROCLEAR ULTRAVUE 2000T MULTIFOCAL TORIC (OMAFLICON A) SOFT (HYDROPHILIC CONTACT LENS)	OPTI-CENTRE LABORATORIES
K010256	01/29/2001	ULTRAVUE/P 2000T, ULTRAVUE/C 2000T (HIOXIFILCON B) SOFT (MULTIFOCAL TORIC) DAILY WEAR CONTACT LENS (CLEAR & BLUE VISIBIL	OPTI-CENTRE LABORATORIES
K001227	04/17/2000	ULTRA VUE 55/P & C (METHAFILCON A) SOFT (MULTIFOCAL, SPHERICAL, & TORIC) DAILY WEAR CONTACT LENS (CLEAR & BLUE VISIBILIT	OPTI-CENTRE LABORATORIES
K992589	08/02/1999	RESOLUTION 5X (SPHERICAL) AND ULTRA GEL 5X (TORIC)(HIOXIFILCON A) SOFT DAILY WEAR CONTACT LENS, (CLEAR & BLUE VISIBILITY	OPTI-CENTRE LABORATORIES
K983496	10/05/1998	RESOLUTION 45 (SPHERICAL) AND ULTRA GEL (TORIC) (HIOXIFILCON B) SOFT DAILY WEAR CONTACT LENS, )CLEAR & BLUE VISIBILITY T	OPTI-CENTRE LABORATORIES
K974599	12/09/1997	ULTRAVUE/P, ULTRALVUE/C (HIOXIFILCON B)) SOFT (MULTIFOCAL) DAILY WEAR CONTACT LENS (CLEAR & YINTED, LATHE-CUT FROM LENS)	OPTI-CENTRE LABORATORIES