GE Medical Systems - FDA 510(k) Cleared Devices

GE Medical Systems has 167 FDA 510(k) cleared radiology devices. Based in Milwaukee, US.

Latest FDA clearance: Aug 2026. Active since 1989.

Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Tuv Rheinland of North America, Inc. and Intertek Testing Services.