Medical Device Manufacturer · US , Deer Field , IL

Capsule Technologie - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2001

Total

Cleared

Denied

Capsule Technologie has 5 FDA 510(k) cleared medical devices. Based in Deer Field, US.

Historical record: 5 cleared submissions from 2001 to 2019. Primary specialty: Cardiovascular.

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

FDA 510(k) cleared devices by Capsule Technologie

5 devices

1-5 of 5