Deepvoxel, Inc. - FDA 510(k) Cleared Devices

Deepvoxel, Inc. has 1 FDA 510(k) cleared medical devices. Based in Irvine, US.

Last cleared in 2021. Active since 2021. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Deepvoxel, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Albert Rego, PhD, Inc. as regulatory consultant.