# Sumitomo Electric Industries, Inc.

- Location (FDA's records): Walker, MI
- FDA decisions: 2 (1981–1985): 2 510(k) clearances
- Product codes: KLK (2)
- 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
- K852959: PO-510 TCPO2 Monitor (Nov 29, 1985)
- K811836: PO-200 Blood Oxygen Monitor (Jul 27, 1981)

Source page: https://510kreport.com/company/sumitomo-electric-industries