Kofu Factory of Terumo Corp. is one of 71 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
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.
Kofu Factory of Terumo Corp. — FDA 510(k) Products and Clearance History
4 devices
Cleared
Aug 05, 2014
Terumo Pen Injector Needle 34
General Hospital
158d
Cleared
May 30, 2014
SURFLASH SAFETY I.V. CATHETER
General Hospital
28d
Cleared
Nov 02, 2012
SURFFLASH(R) PLUS SAFETY I.V. CATHETER
General Hospital
14d
Cleared
Nov 23, 2005
TERUMO MICRO TAPERED PEN NEEDLE
General Hospital
65d