Cgx, LLC - FDA 510(k) Cleared Devices

Cgx, LLC has 1 FDA 510(k) cleared medical devices. Based in San Diego, US.

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

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

510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.