Medical Device Manufacturer · US , Crofton , MD

Smith - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1997

Total

Cleared

Denied

Smith has 5 FDA 510(k) cleared medical devices. Based in Crofton, US.

Historical record: 5 cleared submissions from 1997 to 1998. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Smith Filter by specialty or product code using the sidebar.

Smith is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Smith

5 devices

1-5 of 5