Ge Healthcare Technologies is one of 16529 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ge Healthcare Technologies - FDA 510(k) Cleared Devices
Recent clearances: GE HEALTHCARE INSTA TRAK 3500PLUS/ FLUORO TRAK 9800 PLUS SYSTEM WITH AXCESS BONE PIN, MODEL PART # 1006955, AMX5 AND AMX5D MOBILE X-RAY SYSTEMS
2
Total
2
Cleared
0
Denied
Ge Healthcare Technologies has 2 FDA 510(k) cleared medical devices. Based in Milwaukee, US.
Historical record: 2 cleared submissions from 2004 to 2005. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Ge Healthcare Technologies Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Rheinland of North America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Ge Healthcare Technologies
2 devices