Therataxis, LLC - FDA 510(k) Cleared Devices

Therataxis, LLC has 1 FDA 510(k) cleared medical devices. Based in Baltimore, US.

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

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

510(k) submissions have been managed by Convergent Clinical,Inc. as regulatory consultant.