Keisei (Usa) Co., Ltd.

Keisei (Usa) Co., Ltd. holds 2 FDA 510(k) medical device clearances, first cleared 1993, most recent 1996.

Top product codes for Keisei (Usa) Co., Ltd.

CAE — Anesthesiology1 device
FNM — General Hospital1 device

Recent clearances by Keisei (Usa) Co., Ltd.

K950613 — KEISEICode CAE·1996-02-14
K925651 — LIFE ISLAND 21Code FNM·1993-07-27

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