Terumo Clinical Supply Co., Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Terumo Clinical Supply Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Kakamigahara, JP.
Last cleared in 2021. Active since 2021. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Terumo Clinical Supply Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Terumo Medical Corporation as regulatory consultant.
1 devices