This page includes the latest FDA filings for Bausch Lomb Inc 50 Technology Driveirvine Ca 92618 Pma Numberp060022 Supplement Numbers030 Date Received08 16 2022 Decision Date09 20 2022 Product Code Hql 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.
Device Company | Device | Date |
|---|---|---|
| Bausch & Lomb, Inc.50 Technology Driveirvine, CA 92618 PMA NumberP060022 Supplement NumberS030 Date Received08/16/2022 Decision Date09/20/2022 Product Code HQL Advisory Committee Ophthalmic Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No | Akreos® Posterior Chamber Intraocular Lens (IOL) | 2022-09-20 |