Medical Device Manufacturer · US , Waukesha , WI

General Electric Medical Systems - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2001

Total

Cleared

Denied

General Electric Medical Systems has 6 FDA 510(k) cleared medical devices. Based in Waukesha, US.

Historical record: 6 cleared submissions from 2001 to 2005. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by General Electric Medical Systems 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.

General Electric Medical Systems is one of 23663 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - General Electric Medical Systems

6 devices

1-6 of 6

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Sep 25, 2026