Johnson Johnson Surgical Vision Inc 31 Technology Drivesuite 200irvine Ca 92618 Pma Numberp990080 Supplement Numbers056 Date Received11 09 2022 Decision Date12 06 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 Johnson Johnson Surgical Vision Inc 31 Technology Drivesuite 200irvine Ca 92618 Pma Numberp990080 Supplement Numbers056 Date Received11 09 2022 Decision Date12 06 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
Johnson & Johnson Surgical Vision, Inc.31 Technology Drivesuite 200irvine, CA 92618 PMA NumberP990080 Supplement NumberS056 Date Received11/09/2022 Decision Date12/06/2022 Product Code HQL  Advisory Committee Ophthalmic Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
 TECNIS® Foldable Acrylic IOL2022-12-06

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