Ge Healthcare Information Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ge Healthcare Information Technologies, Inc. - FDA 510(k) Cleared Dev...
Recent clearances: Mac-Lab Recording Systems AltiX, CardioLab Recording Systems AltiX, ComboLab Recording Systems AltiX, MLCL Client Software AltiX
1
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1
Cleared
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Denied
Ge Healthcare Information Technologies, Inc. has 1 FDA 510(k) cleared medical devices. Based in Wauwatosa, US.
Last cleared in 2022. Active since 2022. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Ge Healthcare Information Technologies, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Ge Healthcare Information Technologies, Inc.
1 devices