Keisei (Usa) Co., Ltd. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Keisei (Usa) Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Torrance, US.
Historical record: 2 cleared submissions from 1993 to 1996. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Keisei (Usa) Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Keisei (Usa) Co., Ltd.
2 devices