Medical Device Manufacturer · IT , Due Carrare Padova

Artiglass Srl - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2013

Total

Cleared

Denied

Artiglass Srl has 2 FDA 510(k) cleared medical devices. Based in Due Carrare Padova, IT.

Last cleared in 2022. Active since 2013. Primary specialty: Anesthesiology.

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

FDA 510(k) cleared devices by Artiglass Srl

2 devices

1-2 of 2