Medical Device Manufacturer · DE , Erlangen

Pausch Medical GmbH

3 submissions · 3 cleared · Since 2016
3
Total
3
Cleared
0
Denied

Pausch Medical GmbH — FDA 510(k) Submissions

Pausch Medical GmbH has submitted 3 FDA 510(k) premarket notifications since 2016, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, X-ray, Fluoroscopic, Image-intensified, System, X-ray, Tomographic . Use the specialty filter in the sidebar to narrow results.

3 devices
1–3 of 3
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All3 Radiology 3