Medical Device Manufacturer · US , Walnut Creek , CA

Acorn Group, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1990

Total

Cleared

Denied

Acorn Group, Inc. has 4 FDA 510(k) cleared medical devices. Based in Walnut Creek, US.

Historical record: 4 cleared submissions from 1990 to 1992. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) Regulatory Record - Acorn Group, Inc.

4 devices

1-4 of 4