# Swiss Ray Medical Systems

- Location (FDA's records): Mobile, AL
- FDA decisions: 3 (1992–1992): 3 510(k) clearances
- Product codes: KPR (2), IZO (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K922813: Gen-X 800-400 -- Modification (Aug 11, 1992)
- K921539: GEN-X 800/6/50 (Aug 11, 1992)
- K915227: GEN-X 800/500 (Jan 9, 1992)

Source page: https://510kreport.com/company/swiss-ray-medical-systems