Medical Device Manufacturer · DE , Jungingen

Rud Riester GmbH & CO KG - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1994
4
Total
4
Cleared
0
Denied

Rud Riester GmbH & CO KG has 4 FDA 510(k) cleared medical devices. Based in Jungingen, DE.

Historical record: 4 cleared submissions from 1994 to 1994. Primary specialty: Cardiovascular.

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

FDA 510(k) Regulatory Record - Rud Riester GmbH & CO KG

4 devices
1-4 of 4
Filters
All4 Cardiovascular 4