Medical Device Manufacturer · NL , Gemert

Vitascore B.V. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2007

Total

Cleared

Denied

Vitascore B.V. has 1 FDA 510(k) cleared medical devices. Based in Gemert, NL.

Historical record: 1 cleared submissions from 2007 to 2007. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Vitascore B.V.

1 devices

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