Lk Consulting Group is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lk Consulting Group - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Lk Consulting Group has 1 FDA 510(k) cleared medical devices. Based in Anaheim, US.
Historical record: 1 cleared submissions from 2013 to 2013. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Lk Consulting Group Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lk Consulting Group
1 devices