Medical Device Manufacturer · US , Mchenry , IL

Actus, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1977

Total

Cleared

Denied

Actus, Inc. has 4 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 4 cleared submissions from 1977 to 1978. Primary specialty: Radiology.

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

FDA 510(k) Regulatory Record - Actus, Inc.

4 devices

1-4 of 4