Rex Medical
Rex Medical holds FDA 510(k) medical device clearances, first cleared 2003, most recent 2012.
Top product codes for Rex Medical
Recent clearances by Rex Medical
- K120346 — CLEANER ROTATIONAL THROMBECTOMY SYSTEM
- K113103 — SPLITWIRE PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY SCORING DEVICE
- K102043 — ULTRASTREAM CHRONIC HEMODIALYSIS CATHETER
- K091029 — CLEANER ROTATIONAL THROMBECTOMY SYSTEM (9 MM X 65 CM) AND (9 MM X 120 CM)
- K081410 — OPTION VENA CAVA FILTER
- K071422 — 15.5F HEMO-STREAM HEMODIALYSIS CATHETER SET
- K051468 — INNER-LOCK INTRODUCER SHEATH
- K040252 — CLEANER ROTATIONAL THROMBECTOMY SYSTEM KIT
- K033793 — CLEANER II ROTATIONAL THROMBECTOMY SYSTEM
- K032569 — SHORT INTRODUCER SHEATH
- K031610 — REX MEDICAL CLEANER ROTATIONAL THROMBECTOMY SYSTEM
- K023847 — HEMO-STREAM HEMODIALYSIS CATHETER SET
- K022170 — INNER-LOCK LOCKING INTRODUCER SHEATHS
Data sourced from openFDA. This site is unofficial and independent of the FDA.