Powerbasetec GmbH - FDA 510(k) Cleared Devices

Powerbasetec GmbH has 1 FDA 510(k) cleared medical devices. Based in Bodensee, DE.

Last cleared in 2022. Active since 2022. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Powerbasetec GmbH Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Qip GmbH as regulatory consultant.