Clarus Viewer Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Clarus Viewer Corporation - FDA 510(k) Cleared Devices
Recent clearances: Clarus Viewer
1
Total
1
Cleared
0
Denied
Clarus Viewer Corporation has 1 FDA 510(k) cleared medical devices. Based in Huntsville, US.
Last cleared in 2023. Active since 2023. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Clarus Viewer Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Kapstone Medical, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Clarus Viewer Corporation
1 devices