Terumo Medical Corporation950 Elkton Blvd Elkton Md 21921 Pma Numberp930038 Supplement Numbers100 Date Received07 28 2022 Decision Date08 26 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 Terumo Medical Corporation950 Elkton Blvd Elkton Md 21921 Pma Numberp930038 Supplement Numbers100 Date Received07 28 2022 Decision Date08 26 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 Filings

Device Company	Device	Date
PMA P930038S100 TERUMO MEDICAL CORPORATION950 Elkton Blvd.elkton, MD 21921 PMA NumberP930038 Supplement NumberS100 Date Received07/28/2022 Decision Date08/26/2022 Product Code MGB  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	ANGIO-SEAL VIP Vascular Closure	2022-08-26