Grason Stadler is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Grason Stadler - FDA 510(k) Cleared Devices
Recent clearances: GSI Audera Pro
1
Total
1
Cleared
0
Denied
Grason Stadler has 1 FDA 510(k) cleared medical devices. Based in Eden Prairie, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Grason Stadler Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Kamm & Associates as regulatory consultant.
FDA 510(k) Regulatory Record - Grason Stadler
1 devices