Kofu Factory of Terumo Corp. is one of 148 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.
Kofu Factory of Terumo Corp. - FDA 510(k) Cleared Devices
Recent clearances: Terumo Pen Injector Needle 34, SURFLASH SAFETY I.V. CATHETER, SURFFLASH(R) PLUS SAFETY I.V. CATHETER
4
Total
4
Cleared
0
Denied
Kofu Factory of Terumo Corp. has 4 FDA 510(k) cleared medical devices. Based in Nakakoma-Gun, Yamanashi, JP.
Historical record: 4 cleared submissions from 2005 to 2014. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Kofu Factory of Terumo Corp. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Kofu Factory of Terumo Corp.
4 devices