Bausch Lomb Inc 14853 Deveau Placeminnetonka Mn 55345 Pma Numberp850068 Supplement Numbers014 Date Received02 01 2022 Decision Date03 18 2022 Product Code Lpm 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 Inc 14853 Deveau Placeminnetonka Mn 55345 Pma Numberp850068 Supplement Numbers014 Date Received02 01 2022 Decision Date03 18 2022 Product Code Lpm 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, Inc.14853 Deveau Placeminnetonka, MN 55345 PMA NumberP850068 Supplement NumberS014 Date Received02/01/2022 Decision Date03/18/2022 Product Code LPM  Advisory Committee Ophthalmic Supplement Typenormal 180 Day Track Supplement Reason Change Design/components/specifications/material Expedited Review Granted? No
SILSOFT (ELASTOFILCON A) CONTACT LENSES2022-03-18

Related Finance Registrations

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.