Alcon Laboratories6201 South Freeway R3 48fort Worth Tx 76134 Pma Numberp950018 Supplement Numbers021 Date Received07 18 2022 Decision Date08 12 2022 Product Code Lwl 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 Freeway R3 48fort Worth Tx 76134 Pma Numberp950018 Supplement Numbers021 Date Received07 18 2022 Decision Date08 12 2022 Product Code Lwl 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 Registration(s)

FDA Filings

Device
Company
DeviceDate
ALCON LABORATORIES6201 South Freeway R3-48fort Worth, TX 76134 PMA NumberP950018 Supplement NumberS021 Date Received07/18/2022 Decision Date08/12/2022 Product Code LWL  Advisory Committee Ophthalmic Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
Perfluoron™2022-08-12

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