# Ge Medical Systems W-400

- Location (FDA's records): Waukesha, WI
- FDA decisions: 1 (2003–2003): 1 510(k) clearance
- Product codes: LLZ (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 9 (0 its own)
- Recalls linked to its devices: 6 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- GE Medical Systems: 1 (https://510kreport.com/company/ge-medical-systems)

## Firms that cite its devices most
- Confirma, Inc.: 1 (https://510kreport.com/company/confirma)
- Dr Systems, Inc.: 1 (https://510kreport.com/company/dr-systems)
- Ge Medical Systems Information Technologies: 1 (https://510kreport.com/company/ge-medical-systems-information-technologies)
- Philips Medical Systems Nederland B.V.: 1 (https://510kreport.com/company/philips-medical-systems-nederland)
- Agfa Corp.: 1 (https://510kreport.com/company/agfa)
- Hologic, Inc.: 1 (https://510kreport.com/company/hologic)
- Three Palm Software, LLC: 1 (https://510kreport.com/company/three-palm-software)
- American Medical Sales, Inc.: 1 (https://510kreport.com/company/american-medical-sales)

## Its most-cited devices
- K033400: Seno Advantage (2003), cited by 9

## Recent decisions
- K033400: Seno Advantage (Dec 4, 2003)

Source page: https://510kreport.com/company/ge-medical-systems-w-400