Visura Technologies, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Visura Technologies, LLC - FDA 510(k) Cleared Devices
Recent clearances: Visura Technologies TEECAD System
1
Total
1
Cleared
0
Denied
Visura Technologies, LLC has 1 FDA 510(k) cleared medical devices. Based in Evanston, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Visura Technologies, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Valleygrey Enterprise as regulatory consultant.
FDA 510(k) Regulatory Record - Visura Technologies, LLC
1 devices