Abbott Vascular Inc 3200 Lakeside Drivesanta Clara Ca 95054 Pma Numberp040038 Supplement Numbers040 Date Received06 14 2022 Decision Date07 13 2022 Product Code Nim 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 Vascular Inc 3200 Lakeside Drivesanta Clara Ca 95054 Pma Numberp040038 Supplement Numbers040 Date Received06 14 2022 Decision Date07 13 2022 Product Code Nim 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 VASCULAR INC.3200 Lakeside Drivesanta Clara, CA 95054 PMA NumberP040038 Supplement NumberS040 Date Received06/14/2022 Decision Date07/13/2022 Product Code NIM  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
XACT Carotid Stent System2022-07-13

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