Medical Device Manufacturer · IT , Vicenza

Sit Sordina Iort Technologies Spa - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2018

Recent clearances: LIAC S, LIAC HWL

2
Total
2
Cleared
0
Denied

Sit Sordina Iort Technologies Spa has 2 FDA 510(k) cleared medical devices. Based in Vicenza, IT.

Historical record: 2 cleared submissions from 2018 to 2019. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Sit Sordina Iort Technologies Spa 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 - Sit Sordina Iort Technologies Spa

2 devices
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