Alcon Laboratories6201 South Freewayfort Worth Tx 76134 Pma Numberp990023 Supplement Numbers017 Date Received08 23 2022 Decision Date09 15 2022 Product Code Lzp Advisory Committee Ophthalmic Supplement Type30 Day Notice Supplement Reason Process Change Manufacturer Sterilizer Packager Supplier Expedited Review Granted No

FDA Filings

This page includes the latest FDA filings for Alcon Laboratories6201 South Freewayfort Worth Tx 76134 Pma Numberp990023 Supplement Numbers017 Date Received08 23 2022 Decision Date09 15 2022 Product Code Lzp Advisory Committee Ophthalmic Supplement Type30 Day Notice Supplement Reason Process 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 P990023S017 ALCON LABORATORIES6201 South Freewayfort Worth, TX 76134 PMA NumberP990023 Supplement NumberS017 Date Received08/23/2022 Decision Date09/15/2022 Product Code LZP  Advisory Committee Ophthalmic Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	CELLUGEL OVD	2022-09-15