Medical Device Manufacturer · DE , Jungingen

Rudolf Riester GmbH - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2017

Total

Cleared

Denied

Rudolf Riester GmbH has 3 FDA 510(k) cleared medical devices. Based in Jungingen, DE.

Historical record: 3 cleared submissions from 2017 to 2019. Primary specialty: Cardiovascular.

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

FDA 510(k) cleared devices by Rudolf Riester GmbH

3 devices

1-3 of 3