Hologic Inc 1240 Elko Drivesunnyvale Ca 94089 Pma Numberp920048 Supplement Numbers022 Date Received03 31 2022 Decision Date04 13 2022 Product Code Lkv Advisory Committee Toxicology 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 Hologic Inc 1240 Elko Drivesunnyvale Ca 94089 Pma Numberp920048 Supplement Numbers022 Date Received03 31 2022 Decision Date04 13 2022 Product Code Lkv Advisory Committee Toxicology 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 P920048S022 HOLOGIC, INC.1240 Elko Drivesunnyvale, CA 94089 PMA NumberP920048 Supplement NumberS022 Date Received03/31/2022 Decision Date04/13/2022 Product Code LKV  Advisory Committee Toxicology Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	Rapid fFN for the TLiIQ System	2022-04-13