FDA 510(k) Applications Submitted by KATHLEEN JOHNSON

FDA 510(k) Number	Submission Date	Device Name	Applicant
K090006	01/02/2009	LIFEBRIDGE B2T, MODEL 7001	LIFEBRIDGE MEDIZINTECHNIK AG
K140314	02/10/2014	WARTIE WART REMOVER	YONMEDICAL BV
K020515	02/15/2002	JOSTRA ANTEGRADE CARDIOPLEGIA CANNULA	JOSTRA AG
K020784	03/11/2002	JOSTRA SINGLE STAGE VENOUS RETURN CATHETERS	JOSTRA AG
K170826	03/20/2017	Perfadex Plus	XVIVO Perfusion AB
K020983	03/27/2002	JOSTRA SUCKERS, MODEL JS	JOSTRA AG
K111384	05/17/2011	LIFEBRIDGE	LIFEBRIDGE MEDIZINTECHNIK AG
K022022	06/20/2002	JOSTRA VENT CATHETERS, MODELS LV & HKV	JOSTRA AG
K012617	08/13/2001	JOSTRA ARTERIAL PERFUSION CANNULAE, MODEL A...	JOSTRA AG
K012774	08/20/2001	JOSTRA ARTERIAL PERFUSION CANNULAE	JOSTRA AG
K002857	09/13/2000	ELS CANNULA (KIT), MODEL M1210-88,M1510-88	JOSTRA AG
K023132	09/20/2002	JOSTRA MECC SYSTEM	JOSTRA AG
K123136	10/05/2012	GENESIS HEALTH RECORD SYSTEM, (GHRS)	GENESIS HEALTH TECHNOLOGIES
K053025	10/27/2005	JOSTRA HLM TUBING SET	MAQUET CARDIOPULMONARY AG
K103357	11/16/2010	LIFEBRIDGE	LIFEBRIDGE MEDIZINTECHNIK AG
K003551	11/17/2000	VENOUS HARDSHELL CARDIOTOMY RESEVOIR, MODEL VHK 4201	JOSTRA AG
K013939	11/29/2001	JOSTRA FLOWPROBE FP-32E	JOSTRA AG
K013944	11/29/2001	JOSTRA DUAL STAGE VENOUS RETURN CANNULAE	JOSTRA AG
K014303	12/31/2001	JOSTRA RETROGRADE CARDIOPLEGIA CANNULAE	JOSTRA AG