Johnson Johnson Surgical Vision Inc 31 Technology Drivesuite 200irvine Ca 92618 Pma Numberp980040 Supplement Numbers152 Date Received10 25 2022 Decision Date11 17 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 Numberp980040 Supplement Numbers152 Date Received10 25 2022 Decision Date11 17 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 Filings

Device Company	Device	Date
PMA P980040S152 Johnson & Johnson Surgical Vision, Inc.31 Technology Drivesuite 200irvine, CA 92618 PMA NumberP980040 Supplement NumberS152 Date Received10/25/2022 Decision Date11/17/2022 Product Code HQL  Advisory Committee Ophthalmic Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	SENSAR® 1-Piece IOL, Model AAB00, TECNIS® Monofocal 1-Piece IOL, Model ZCB00, TECNIS® Multifocal 1-Piece IOL, Model ZMB0	2022-11-17