Ashitaka Factory of Terumo Corp. is one of 143 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
Recent clearances: Radifocus Glidewire, Radifocus Optitorque Angiographic Catheter, CAPIOX FX15 AND FX25 HOLLOW FIBER OXYGENATOR/RESERVOIR
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.
Regulatory submissions have been managed by Terumo Medical Corporation and Terumo Medical Corp..
FDA 510(k) Regulatory Record - Ashitaka Factory of Terumo Corp.
3 devices