Life Technologies Corporation5781 Van Allen Waycarlsbad Ca 92008 Pma Numberp160045 Supplement Numbers036 Date Received03 29 2022 Decision Date08 11 2022 Product Code Pqp Advisory Committee Pathology Supplement Type135 Review Track For 30 Day Notice Supplement Reason Process Change Manufacturer Sterilizer Packager Supplier Expedited Review Granted No

FDA Filings

This page includes the latest FDA filings for Life Technologies Corporation5781 Van Allen Waycarlsbad Ca 92008 Pma Numberp160045 Supplement Numbers036 Date Received03 29 2022 Decision Date08 11 2022 Product Code Pqp Advisory Committee Pathology Supplement Type135 Review Track For 30 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
LIFE TECHNOLOGIES CORPORATION5781 Van Allen Waycarlsbad, CA 92008 PMA NumberP160045 Supplement NumberS036 Date Received03/29/2022 Decision Date08/11/2022 Product Code PQP  Advisory Committee Pathology Supplement Type135 Review Track For 30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
Oncomine Dx Target Test2022-08-11

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