Ge Medical Syst. Information Technologies is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ge Medical Syst. Information Technologies - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Ge Medical Syst. Information Technologies has 2 FDA 510(k) cleared medical devices. Based in Milwaukee, US.
Historical record: 2 cleared submissions from 2004 to 2009. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Ge Medical Syst. Information Technologies Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ge Medical Syst. Information Technologies
2 devices