Venous Health Systems, Inc. is one of 16396 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Venous Health Systems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VASCULAIRE COMPRESSION SYSTEM, VASCULAIRE SLEEVE (FOOT & CALF), VASCULAIRE SLEEVE (CALF), VASCULAIRE COMPRESSION SYSTEM MODEL FLS-0003, VASCULAIRE COMPRESSION SYSTEM
3
Total
3
Cleared
0
Denied
Venous Health Systems, Inc. has 3 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.
Historical record: 3 cleared submissions from 2011 to 2013. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Venous Health Systems, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Venous Health Systems, Inc.
3 devices