Medical Device Manufacturer · US , Doylestown , PA

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

7 submissions · 7 cleared · Since 2006

Total

Cleared

Denied

Neoforce Group, Inc. has 7 FDA 510(k) cleared medical devices. Based in Doylestown, US.

Historical record: 7 cleared submissions from 2006 to 2011. Primary specialty: Anesthesiology.

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

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

7 devices

1-7 of 7