O3 Enterprise Srl is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
O3 Enterprise Srl - FDA 510(k) Cleared Devices
Recent clearances: ZeeroMED View
1
Total
1
Cleared
0
Denied
O3 Enterprise Srl has 1 FDA 510(k) cleared medical devices. Based in Tieste, IT.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by O3 Enterprise Srl Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Sigma Biomedical as regulatory consultant.
FDA 510(k) Regulatory Record - O3 Enterprise Srl
1 devices