Biosense Webster Inc 31 Technology Drivesuite 200irvine Ca 92618 Pma Numberp990071 Supplement Numbers053 Date Received02 16 2022 Decision Date03 15 2022 Product Code Lpb 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 Biosense Webster Inc 31 Technology Drivesuite 200irvine Ca 92618 Pma Numberp990071 Supplement Numbers053 Date Received02 16 2022 Decision Date03 15 2022 Product Code Lpb 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
BIOSENSE WEBSTER, INC.31 Technology Drivesuite 200irvine, CA 92618 PMA NumberP990071 Supplement NumberS053 Date Received02/16/2022 Decision Date03/15/2022 Product Code LPB  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
SmartAblate Irrigation Tubing Set2022-03-15

Related Finance Registrations

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