# Ge Healthcare Information Technologies

- Location (FDA's records): Barrington, IL
- FDA decisions: 2 (2006–2022): 2 510(k) clearances
- Names in FDA's records: Ge Healthcare Information Technologies (1); Ge Healthcare Information Technologies, Inc. (1)
- Product codes: LLZ (1), DQK (1)
- Predicates its devices cite: 8 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- General Electric Medical Systems: 3 (https://510kreport.com/company/general-electric-medical-systems)
- Ge Medical Systems Information Technologies: 2 (https://510kreport.com/company/ge-medical-systems-information-technologies)
- GE Medical Systems: 2 (https://510kreport.com/company/ge-medical-systems)
- Ge Medical Systems Europe: 1 (https://510kreport.com/company/ge-medical-systems-europe)

## Firms that cite its devices most
- Ge Medical Systems Information Technologies: 1 (https://510kreport.com/company/ge-medical-systems-information-technologies)

## Its most-cited devices
- K213972: Mac-Lab Recording Systems AltiX, CardioLab Recording Systems AltiX, ComboLab Recording Systems AltiX, MLCL Client Software AltiX (2022), cited by 1

## Recent decisions
- K213972: Mac-Lab Recording Systems AltiX, CardioLab Recording Systems AltiX, ComboLab Recording Systems AltiX, MLCL Client Software AltiX (Feb 17, 2022)
- K061372: Centricity AW Suite Option (May 30, 2006)

Source page: https://510kreport.com/company/ge-healthcare-information-technologies