Medical Device Manufacturer · US , Rochester , MN

Compass Intl., Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1995

Total

Cleared

Denied

Compass Intl., Inc. has 2 FDA 510(k) cleared medical devices. Based in Rochester, US.

Historical record: 2 cleared submissions from 1995 to 1997. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Compass Intl., Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Compass Intl., Inc.

2 devices

1-2 of 2