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.

Capsule Technologie is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Capsule Technologie

5 devices

1-5 of 5