Allergan2525 Dupont Dr Irvine Ca 92612 Pma Numberp020056 Supplement Numbers058 Date Received04 01 2022 Decision Date10 05 2022 Product Code Ftr Advisory Committee General Plastic Surgery 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 Allergan2525 Dupont Dr Irvine Ca 92612 Pma Numberp020056 Supplement Numbers058 Date Received04 01 2022 Decision Date10 05 2022 Product Code Ftr Advisory Committee General Plastic Surgery 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
Allergan2525 Dupont Dr.irvine, CA 92612 PMA NumberP020056 Supplement NumberS058 Date Received04/01/2022 Decision Date10/05/2022 Product Code FTR  Advisory Committee General & Plastic Surgery Supplement Type135 Review Track For 30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
NATRELLE Saline-Filled Breast Implants2022-10-05

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