Ashitaka Factory of Terumo Coporation is one of 143 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
Recent clearances: Radifocus Glidewire Advantage Track
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.
510(k) submissions have been managed by Terumo Medical Corporation as regulatory consultant.
FDA 510(k) Regulatory Record - Ashitaka Factory of Terumo Coporation
1 devices