Medical Device Manufacturer · DE , D-72417 Jungingen

Rudolf Riester GmbH & Co. KG - FDA 510(k) Cleared Devices

30 submissions · 26 cleared · Since 1993

30

Total

26

Cleared

0

Denied

FDA 510(k) Regulatory Record - Rudolf Riester GmbH & Co. KG General Hospital ✕

1 devices

1-1 of 1

Cleared Dec 09, 1994

H 5100, H 5200, H 5300

General Hospital · 30d