The Smithworks Company is one of 16269 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
The Smithworks Company - FDA 510(k) Cleared Devices
Recent clearances: SOFT SACK IV FLUID WARMER, THE FLOORMOUNT IV FLUID WARMER, THE PAK 2 IV WARMER AND THE THERMAL SAC PRESSURE INFUSER
1
Total
1
Cleared
0
Denied
The Smithworks Company has 1 FDA 510(k) cleared medical devices. Based in Bellevue, US.
Historical record: 1 cleared submissions from 2006 to 2006. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by The Smithworks Company Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - The Smithworks Company
1 devices