Medical Device Manufacturer · IT , Mapello

D.E.A Project S.R.1. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2023

Total

Cleared

Denied

D.E.A Project S.R.1. has 1 FDA 510(k) cleared medical devices. Based in Mapello, IT.

Last cleared in 2023. Active since 2023. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by D.E.A Project S.R.1. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by D.E.A Project S.R.1.

1 devices

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