Shannon Group - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Shannon Group has 2 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 2 cleared submissions from 1981 to 1982. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Shannon Group Filter by specialty or product code using the sidebar.
2 devices