Bausch Lomb Surgical Inc 1400 N Goodman St Rochester Ny 14609 Pma Numberp850059 Supplement Numbers009 Date Received12 19 1988 Decision Date04 11 1990 Withdrawal Date 11 26 2008 Product Code Hql Advisory Committee Ophthalmic Supplement Typenormal 180 Day Track Supplement Reason Change Design Components Specifications Material 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 Numbers009 Date Received12 19 1988 Decision Date04 11 1990 Withdrawal Date 11 26 2008 Product Code Hql Advisory Committee Ophthalmic Supplement Typenormal 180 Day Track Supplement Reason Change Design Components Specifications Material Expedited Review Granted No. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

FDA Filings

Device
Company
DeviceDate
BAUSCH & LOMB SURGICAL, INC.1400 N. Goodman St.rochester, NY 14609 PMA NumberP850059 Supplement NumberS009 Date Received12/19/1988 Decision Date04/11/1990 Withdrawal Date 11/26/2008 Product Code HQL  Advisory Committee Ophthalmic Supplement Typenormal 180 Day Track Supplement Reason Change Design/components/specifications/material Expedited Review Granted? No
 KELMAN(TM) OMNIFIT II MODEL 21001990-04-11

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