Medical Device Manufacturer · US , Mchenry , IL

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

8 submissions · 8 cleared · Since 1981

Total

Cleared

Denied

Accutome, Inc. has 8 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 8 cleared submissions from 1981 to 2015. Primary specialty: Radiology.

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

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

8 devices

1-8 of 8