Medical Device Manufacturer · US , Bothell , WA

Vioguard - FDA 510(k) Cleared Devices

1 submissions · 0 cleared · Since 2011
1
Total
0
Cleared
1
Denied

Vioguard has 0 FDA 510(k) cleared medical devices. Based in Bothell, US.

Active since 2011. Primary specialty: General Hospital.

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

FDA 510(k) Regulatory Record - Vioguard
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