Alcon Laboratories Inc 6201 South Freewayfort Worth Tx 76134 2099 Pma Numberp010019 Supplement Numbers083 Date Received06 09 2022 Decision Date07 06 2022 Product Code Lpm 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 Laboratories Inc 6201 South Freewayfort Worth Tx 76134 2099 Pma Numberp010019 Supplement Numbers083 Date Received06 09 2022 Decision Date07 06 2022 Product Code Lpm 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 Laboratories, Inc.6201 South Freewayfort Worth, TX 76134-2099 PMA NumberP010019 Supplement NumberS083 Date Received06/09/2022 Decision Date07/06/2022 Product Code LPM  Advisory Committee Ophthalmic Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
Lotrafilcon A and B Soft Contact Lenses2022-07-06

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