St Jude Medicalone St Jude Medical Drivest Paul Mn 55117 Pma Numberp130026 Supplement Numbers079 Date Received08 01 2022 Decision Date08 31 2022 Product Code Oae 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 St Jude Medicalone St Jude Medical Drivest Paul Mn 55117 Pma Numberp130026 Supplement Numbers079 Date Received08 01 2022 Decision Date08 31 2022 Product Code Oae 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
St. Jude Medicalone St. Jude Medical Drivest. Paul, MN 55117 PMA NumberP130026 Supplement NumberS079 Date Received08/01/2022 Decision Date08/31/2022 Product Code OAE  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
TactiCath™ Contact Force Ablation Catheter, Sensor Enabled™2022-08-31

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