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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
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