Medical Device Manufacturer · US , Andover , MA

Capsule Technologie Sas - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2015

Total

Cleared

Denied

Capsule Technologie Sas has 4 FDA 510(k) cleared medical devices. Based in Andover, US.

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

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

FDA 510(k) cleared devices by Capsule Technologie Sas

4 devices

1-4 of 4