Bausch Lomb Inc 50 Technologyirvine Ca 92618 Pma Numberp840039 Supplement Numbers064 Date Received07 11 2022 Decision Date08 09 2022 Product Code Hql 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 Bausch Lomb Inc 50 Technologyirvine Ca 92618 Pma Numberp840039 Supplement Numbers064 Date Received07 11 2022 Decision Date08 09 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.

FDA Registration(s)

FDA Filings

Device
Company
DeviceDate
Bausch & Lomb, Inc.50 Technologyirvine, CA 92618 PMA NumberP840039 Supplement NumberS064 Date Received07/11/2022 Decision Date08/09/2022 Product Code HQL  Advisory Committee Ophthalmic Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
PMMA Anterior Chamber Intraocular Lenses2022-08-09

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