Sumitomo Electric Industries, Inc.

Sumitomo Electric Industries, Inc. holds 2 FDA 510(k) medical device clearances, first cleared 1981, most recent 1985.

Top product codes for Sumitomo Electric Industries, Inc.

KLK — Anesthesiology2 devices

Recent clearances by Sumitomo Electric Industries, Inc.

K852959 — PO-510 TCPO2 MONITORCode KLK·1985-11-29
K811836 — PO-200 BLOOD OXYGEN MONITORCode KLK·1981-07-27

Data sourced from openFDA. This site is unofficial and independent of the FDA.