# Ge Medical Systems Ultrasound and Primary Care Diagnostic,

- Location (FDA's records): Wauwatosa, WI
- FDA decisions: 2 (2023–2023): 2 510(k) clearances
- Product codes: IYN (2)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- GE Healthcare: 1 (https://510kreport.com/company/ge-healthcare)
- GE Medical Systems Ultrasound and Primary Care Diagnostics: 1 (https://510kreport.com/company/ge-medical-systems-ultrasound-and-primary-care-diagnostics)

## Firms that cite its devices most
- GE Medical Systems Ultrasound and Primary Care Diagnostics: 4 (https://510kreport.com/company/ge-medical-systems-ultrasound-and-primary-care-diagnostics)

## Its most-cited devices
- K231989: LOGIQ E10s, LOGIQ Fortis (2023), cited by 3
- K232186: LOGIQ e (2023), cited by 1

## Recent decisions
- K231989: LOGIQ E10s, LOGIQ Fortis (Nov 7, 2023)
- K232186: LOGIQ e (Nov 3, 2023)

Source page: https://510kreport.com/company/ge-medical-systems-ultrasound-and-primary-care-diagnostic