Abbott Vascular3200 Lakeside Drivesanta Clara Ca 95054 Pma Numberp110001 Supplement Numbers018 Date Received02 28 2022 Decision Date03 24 2022 Product Code Nin Advisory Committee Cardiovascular 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 Abbott Vascular3200 Lakeside Drivesanta Clara Ca 95054 Pma Numberp110001 Supplement Numbers018 Date Received02 28 2022 Decision Date03 24 2022 Product Code Nin Advisory Committee Cardiovascular 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 Registration(s)

FDA Filings

Device
Company
DeviceDate
ABBOTT VASCULAR3200 Lakeside Drivesanta Clara, CA 95054 PMA NumberP110001 Supplement NumberS018 Date Received02/28/2022 Decision Date03/24/2022 Product Code NIN  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
RX Herculink Elite Renal Stent System2022-03-24

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