Pausch Medical GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Pausch Medical GmbH - FDA 510(k) Cleared Devices
Recent clearances: Ortho Device, ADAPTIX 3D Orthopedic Imaging System, Uroview FD II
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.
FDA 510(k) Regulatory Record - Pausch Medical GmbH
3 devices