South Dakota Partners is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
South Dakota Partners - FDA 510(k) Cleared Devices
Recent clearances: EZ-STIK Electrodes
1
Total
1
Cleared
0
Denied
South Dakota Partners has 1 FDA 510(k) cleared medical devices. Based in Clear Lake, US.
Last cleared in 2023. Active since 2023. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by South Dakota Partners Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - South Dakota Partners
1 devices