Pausch Medical GmbH - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Pausch Medical GmbH has 3 FDA 510(k) cleared medical devices. Based in Erlangen, DE.
Last cleared in 2023. Active since 2016. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Pausch Medical GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Emergo Global Consulting, LLC as regulatory consultant.
3 devices