Medical Device Manufacturer · US , Anaheim , CA

LK Consulting Group USA, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2014

Total

Cleared

Denied

LK Consulting Group USA, Inc. has 3 FDA 510(k) cleared medical devices. Based in Anaheim, US.

Historical record: 3 cleared submissions from 2014 to 2015. Primary specialty: Dental.

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

FDA 510(k) Regulatory Record - LK Consulting Group USA, Inc.

3 devices

1-3 of 3