Medical Device Manufacturer · US , Mchenry , IL

Shannon Group - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1981
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.

FDA 510(k) Regulatory Record - Shannon Group
2 devices
1-2 of 2
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