Barry S. Smith Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Barry S. Smith Co. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Barry S. Smith Co. has 1 FDA 510(k) cleared medical devices. Based in Sacramento, US.
Historical record: 1 cleared submissions from 1989 to 1989. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Barry S. Smith Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Barry S. Smith Co.
1 devices