Kyoto Daiichi Kagaku Co., Ltd.

Kyoto Daiichi Kagaku Co., Ltd. holds 3 FDA 510(k) medical device clearances, first cleared 1982, most recent 1988.

Top product codes for Kyoto Daiichi Kagaku Co., Ltd.

KQO — Clinical Chemistry2 devices
LFR — Clinical Chemistry1 device

Recent clearances by Kyoto Daiichi Kagaku Co., Ltd.

K870708 — GLUCOSCOT II BLOOD GLUCOSE TEST SYSTEMCode LFR·1988-02-02
K870526 — SUPER URINE ANALYZER SYSTEMCode KQO·1987-03-06
K813056 — AUTOMATED URINALYSIS SYSTEMCode KQO·1982-05-05

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