Medical Device Manufacturer · FR , Strasbourg

Visible Patient, Sas - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2015
2
Total
2
Cleared
0
Denied

Visible Patient, Sas has 2 FDA 510(k) cleared medical devices. Based in Strasbourg, FR.

Last cleared in 2021. Active since 2015. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Visible Patient, Sas Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.

FDA 510(k) Regulatory Record - Visible Patient, Sas
2 devices
1-2 of 2
Filters
All2 Radiology 2