FDA 510(k) Applications Submitted by KOFU FACTORY OF TERUMO CORP.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K052561	09/19/2005	TERUMO MICRO TAPERED PEN NEEDLE	KOFU FACTORY OF TERUMO CORP.
K140516	02/28/2014	Terumo Pen Injector Needle 34	KOFU FACTORY OF TERUMO CORP.
K141138	05/02/2014	SURFLASH SAFETY I.V. CATHETER	KOFU FACTORY OF TERUMO CORP.
K123267	10/19/2012	SURFFLASH(R) PLUS SAFETY I.V. CATHETER	KOFU FACTORY OF TERUMO CORP.