Rudolf Riester GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Rudolf Riester GmbH - FDA 510(k) Cleared Devices
Recent clearances: Oscillometric Blood Pressure Monitor
3
Total
3
Cleared
0
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.
510(k) submissions have been managed by Mid-Link Consulting Co, Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Rudolf Riester GmbH
3 devices