Kyoto Daiichi Kagaku Co., Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kyoto Daiichi Kagaku Co., Ltd. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Kyoto Daiichi Kagaku Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 3 cleared submissions from 1982 to 1988. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Kyoto Daiichi Kagaku Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kyoto Daiichi Kagaku Co., Ltd.
3 devices