Cardiva Medical Inc 2900 Lakeside Drivesuite 160santa Clara Ca 95054 Pma Numberp120016 Supplement Numbers030 Date Received10 11 2022 Decision Date11 08 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 Cardiva Medical Inc 2900 Lakeside Drivesuite 160santa Clara Ca 95054 Pma Numberp120016 Supplement Numbers030 Date Received10 11 2022 Decision Date11 08 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 P120016S030 CARDIVA MEDICAL, INC.2900 Lakeside Drivesuite 160santa Clara, CA 95054 PMA NumberP120016 Supplement NumberS030 Date Received10/11/2022 Decision Date11/08/2022 Product Code MGB  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	Cardiva VASCADE Family	2022-11-08