Ashitaka Factory of Terumo Corp. is one of 66 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.
Ashitaka Factory of Terumo Corp. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Ashitaka Factory of Terumo Corp. has 3 FDA 510(k) cleared medical devices. Based in Fujinomiya Shizuoka, JP.
Historical record: 3 cleared submissions from 2013 to 2015. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Ashitaka Factory of Terumo Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ashitaka Factory of Terumo Corp.
3 devices