Terumo Clinical Supply Co., Ltd. is one of 79 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.
Terumo Clinical Supply Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Progreat Lambda
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.
FDA 510(k) Regulatory Record - Terumo Clinical Supply Co., Ltd.
1 devices