Ashitaka Factory of Terumo Corporation - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Ashitaka Factory of Terumo Corporation has 3 FDA 510(k) cleared medical devices. Based in Fujinomiya Shizuoka, JP.
Last cleared in 2021. Active since 2016. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Ashitaka Factory of Terumo Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Ashitaka Factory of Terumo Corporation
3 devices