Redplane AG is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Redplane AG - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Redplane AG has 1 FDA 510(k) cleared medical devices. Based in Zug, CH.
Historical record: 1 cleared submissions from 2008 to 2008. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Redplane AG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Redplane AG
1 devices