James K. Brannon is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
James K. Brannon - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
James K. Brannon has 2 FDA 510(k) cleared medical devices. Based in Culver City, US.
Historical record: 2 cleared submissions from 1996 to 1996. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by James K. Brannon Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - James K. Brannon
2 devices