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.


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