Cordis Us Corporation14201 Nw 60th Avenuemiami Lakes Fl 33014 Pma Numberp040044 Supplement Numbers092 Date Received06 02 2022 Decision Date06 27 2022 Product Code Mgb 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 Cordis Us Corporation14201 Nw 60th Avenuemiami Lakes Fl 33014 Pma Numberp040044 Supplement Numbers092 Date Received06 02 2022 Decision Date06 27 2022 Product Code Mgb 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
Cordis US Corporation14201 Nw 60th Avenuemiami Lakes, FL 33014 PMA NumberP040044 Supplement NumberS092 Date Received06/02/2022 Decision Date06/27/2022 Product Code MGB  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
MynxGrip Vascular Closure , Mynx Control Vascular Closure (VCD)2022-06-27

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