Medical Device Manufacturer · IT , Rimini Rn

Vupiesse S.R.L - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2020

Total

Cleared

Denied

Vupiesse S.R.L has 1 FDA 510(k) cleared medical devices. Based in Rimini Rn, IT.

Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Vupiesse S.R.L Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Vupiesse S.R.L

1 devices

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