Ge Medical Systems Lunar is one of 16306 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ge Medical Systems Lunar - FDA 510(k) Cleared Devices
Recent clearances: ENCORE 14 SOFTWARE RELEASE FOR THE GE LUNAR DXA BONE DENSITOMETERS, GE LUNAR BODY COMPOSITION SOFTWARE
2
Total
2
Cleared
0
Denied
Ge Medical Systems Lunar has 2 FDA 510(k) cleared medical devices. Based in Madison, US.
Historical record: 2 cleared submissions from 2007 to 2012. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Ge Medical Systems Lunar Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Ge Medical Systems Lunar
2 devices