Riken Keiki Co., Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Riken Keiki Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Wales Center, US.
Historical record: 1 cleared submissions from 1995 to 1995. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Riken Keiki Co., Ltd. Filter by specialty or product code using the sidebar.
1 devices