Ashitaka Factory of Terumo Coporation is one of 63 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.
Ashitaka Factory of Terumo Coporation - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Ashitaka Factory of Terumo Coporation has 1 FDA 510(k) cleared medical devices. Based in Fujinomiya Shizuoka, JP.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Ashitaka Factory of Terumo Coporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ashitaka Factory of Terumo Coporation
1 devices