Dynatronics Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dynatronics Corporation - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Dynatronics Corporation has 1 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Historical record: 1 cleared submissions from 2012 to 2012. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Dynatronics Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dynatronics Corporation
1 devices