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 Anesthesiology
1 devices
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