FDA 510(k) Applications Submitted by EILEEN DORSEY

FDA 510(k) Number	Submission Date	Device Name	Applicant
K130520	02/28/2013	CAPIOX FX15 AND FX25 HOLLOW FIBER OXYGENATOR/RESERVOIR	ASHITAKA FACTORY OF TERUMO CORP.
K140774	03/28/2014	TERUMO CAPIOX FX15 AND FX25 HOLLOW FIBER OXYGENATOR/RESERVOIR	Terumo Cardiovascular Systems Corporation
K071630	06/14/2007	TERUMO 31G THINPRO INSULIN SYRINGE	TERUMO MEDICAL CORP.
K221895	06/30/2022	Terumo Advanced Perfusion System 1	Terumo Cardiovascular Systems Corporation
K082362	08/18/2008	SURSHIELD SAFETY I.V. CATHETER	TERUMO MEDICAL CORP.
K082997	10/08/2008	TERUMO HYBRIA CLOSED SYSTEM SAFETY I.V. CATHETER	TERUMO MEDICAL CORP.
K083834	12/23/2008	TERUMO PALL AL6X ARTERIAL FILTER	TERUMO CARDIOVASCULAR SYSTEMS CORP.
K093992	12/24/2009	TERUMO LAUER LOCK ADAPTER	Terumo Cardiovascular Systems Corporation