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Kyoto Daiichi Kagaku Co., Ltd.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K870708 GLUCOSCOT II BLOOD GLUCOSE TEST SYSTEMLFR1988-02-02 View
510(k) K870526 SUPER URINE ANALYZER SYSTEMKQO1987-03-06 View
510(k) K813056 AUTOMATED URINALYSIS SYSTEMKQO1982-05-05 View
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