Bausch Lomb Surgical Inc 1400 N Goodman St Rochester Ny 14609 Pma Numberp850059 Supplement Numbers007 Date Received05 17 1988 Decision Date03 02 1989 Withdrawal Date 11 26 2008 Product Code Hql Advisory Committee Ophthalmic Supplement Typenormal 180 Day Track Supplement Reason Location Change Manufacturer Sterilizer Packager Supplier Expedited Review Granted No

FDA Filings

This page includes the latest FDA filings for Bausch Lomb Surgical Inc 1400 N Goodman St Rochester Ny 14609 Pma Numberp850059 Supplement Numbers007 Date Received05 17 1988 Decision Date03 02 1989 Withdrawal Date 11 26 2008 Product Code Hql Advisory Committee Ophthalmic Supplement Typenormal 180 Day Track Supplement Reason Location Change Manufacturer Sterilizer Packager Supplier Expedited Review Granted No. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Filings

Device Company	Device	Date
PMA P850059S007 BAUSCH & LOMB SURGICAL, INC.1400 N. Goodman St.rochester, NY 14609 PMA NumberP850059 Supplement NumberS007 Date Received05/17/1988 Decision Date03/02/1989 Withdrawal Date 11/26/2008 Product Code HQL  Advisory Committee Ophthalmic Supplement Typenormal 180 Day Track Supplement Reason Location Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	CELMAN(TM) OMNIFIT II MODEL 2100	1989-03-02