Echolight S.P.A is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Echolight S.P.A - FDA 510(k) Cleared Devices
Recent clearances: EchoSK and EchoSGyn modules for EchoS Family devices, EchoS Family, EchoS
3
Total
3
Cleared
0
Denied
Echolight S.P.A has 3 FDA 510(k) cleared medical devices. Based in Lecce, IT.
Last cleared in 2022. Active since 2018. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Echolight S.P.A Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Isemed S.R.L. as regulatory consultant.
FDA 510(k) Regulatory Record - Echolight S.P.A
3 devices