FDA 510(k) Applications Submitted by REX MEDICAL

FDA 510(k) Number	Submission Date	Device Name	Applicant
K081410	05/20/2008	OPTION VENA CAVA FILTER	REX MEDICAL
K102043	07/20/2010	ULTRASTREAM CHRONIC HEMODIALYSIS CATHETER	REX MEDICAL
K120346	02/03/2012	CLEANER ROTATIONAL THROMBECTOMY SYSTEM	REX MEDICAL
K040252	02/04/2004	CLEANER ROTATIONAL THROMBECTOMY SYSTEM KIT	REX MEDICAL
K091029	04/10/2009	CLEANER ROTATIONAL THROMBECTOMY SYSTEM (9 MM X 65 CM) AND (9 MM X 120 CM)	REX MEDICAL
K031610	05/22/2003	REX MEDICAL CLEANER ROTATIONAL THROMBECTOMY SYSTEM	REX MEDICAL
K071422	05/22/2007	15.5F HEMO-STREAM HEMODIALYSIS CATHETER SET	REX MEDICAL
K051468	06/03/2005	INNER-LOCK INTRODUCER SHEATH	REX MEDICAL
K022170	07/03/2002	INNER-LOCK LOCKING INTRODUCER SHEATHS	REX MEDICAL
K032569	08/20/2003	SHORT INTRODUCER SHEATH	REX MEDICAL
K113103	10/19/2011	SPLITWIRE PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY SCORING DEVICE	REX MEDICAL
K023847	11/19/2002	HEMO-STREAM HEMODIALYSIS CATHETER SET	REX MEDICAL
K033793	12/05/2003	CLEANER II ROTATIONAL THROMBECTOMY SYSTEM	REX MEDICAL