Abbott Vascular Devices3200 Lakeside Drivesanta Clara Ca 95054 Pma Numberp050007 Supplement Numbers043 Date Received11 21 2022 Decision Date01 31 2023 Product Code Mgb Advisory Committee Cardiovascular 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 Abbott Vascular Devices3200 Lakeside Drivesanta Clara Ca 95054 Pma Numberp050007 Supplement Numbers043 Date Received11 21 2022 Decision Date01 31 2023 Product Code Mgb Advisory Committee Cardiovascular 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
ABBOTT VASCULAR DEVICES3200 Lakeside Drivesanta Clara, CA 95054 PMA NumberP050007 Supplement NumberS043 Date Received11/21/2022 Decision Date01/31/2023 Product Code MGB  Advisory Committee Cardiovascular Supplement Type135 Review Track For 30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
StarClose SE Vascular Closure System2023-01-31

Related Finance Registrations

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.