Venturemed Group is one of 4788 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Venturemed Group - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Venturemed Group has 1 FDA 510(k) cleared medical devices. Based in Sylvania, US.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Venturemed Group Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Venturemed Group
1 devices