Medical Device Manufacturer · US , Plano , TX

Vedi Corp. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2004

Total

Cleared

Denied

Vedi Corp. has 1 FDA 510(k) cleared medical devices. Based in Plano, US.

Historical record: 1 cleared submissions from 2004 to 2004. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Vedi Corp.

1 devices

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