Smith & Nephew Equipment Group - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Smith & Nephew Equipment Group has 2 FDA 510(k) cleared medical devices. Based in St. Louis, US.
Historical record: 2 cleared submissions from 1991 to 1991. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Smith & Nephew Equipment Group Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Smith & Nephew Equipment Group
2 devices