Richter & Rothe AG is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Richter & Rothe AG - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Richter & Rothe AG has 1 FDA 510(k) cleared medical devices. Based in Leipzig, DE.
Historical record: 1 cleared submissions from 2006 to 2006. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Richter & Rothe AG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Richter & Rothe AG
1 devices