Medical Device Manufacturer · US , Twinsburg , OH

Gvi Technology Partners - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2003
3
Total
3
Cleared
0
Denied

Gvi Technology Partners has 3 FDA 510(k) cleared medical devices. Based in Twinsburg, US.

Historical record: 3 cleared submissions from 2003 to 2007. Primary specialty: Radiology.

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

FDA 510(k) Regulatory Record - Gvi Technology Partners
3 devices
1-3 of 3
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All3 Radiology 3