Bausch Lomb Ireland Limited400 Somerset Corporate Blvdbridgewater Nj 08807 Pma Numberp050026 Supplement Numbers002 Date Received09 04 2020 Decision Date01 20 2023 Product Code Mvf 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 Ireland Limited400 Somerset Corporate Blvdbridgewater Nj 08807 Pma Numberp050026 Supplement Numbers002 Date Received09 04 2020 Decision Date01 20 2023 Product Code Mvf 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 Filings

Device Company	Device	Date
PMA P050026S002 Bausch + Lomb Ireland Limited400 Somerset Corporate Blvdbridgewater, NJ 08807 PMA NumberP050026 Supplement NumberS002 Date Received09/04/2020 Decision Date01/20/2023 Product Code MVF  Advisory Committee Ophthalmic Supplement Typenormal 180 Day Track Supplement Reason Change Design/components/specifications/material Expedited Review Granted? No	Qcellus Laser, Activis Laser, ZSL30 ACT, ZSL120 ACT, and HSBMBQ ACT Slit Lamp Adapters	2023-01-20