Horizon Medical Products, Inc.
Horizon Medical Products, Inc. holds FDA 510(k) medical device clearances, first cleared 1994, most recent 2003.
Top product codes for Horizon Medical Products, Inc.
Recent clearances by Horizon Medical Products, Inc.
- K033473 — MODIFICATION TO VORTEX MP VASCULAR ACCESS PORT
- K032754 — VORTEX MP
- K032557 — TRIUMPH VTX WITH LIFEVALVE CATHETER
- K031718 — LIFEVALVE CENTRAL VENOUS CATHTER
- K022905 — LIFEJET F16 HEMODIALYSIS/APHERESIS CHRONIC CATHETER
- K013871 — LIFEGUARD SAFETY INFUSION SET
- K011916 — SUPER C HEMODIALYSIS/APHERESIS CHRONIC CATHETER, MODEL DC-36 SERIES, DC-40 SERIES, DC-45 SERIES
- K010767 — LIFEPORT VTX ACCESS SYSTEM,MODEL VTX 7000 SERIES
- K010189 — VORTEX ACCESS SYSTEM
- K994196 — HORIZON MEDICAL PRODUCTS MICROPORT 2 PERIPHERAL ACCESS PORT SYSTEM
- K951814 — TRIUMPH-1 PORT
- K933986 — HMP POLYSULFONE PORT
- K933990 — HMP TITANIUM PORT
- K934504 — HMP DUAL TITANIUM PORT
- K934573 — HMP TITANIUM LOW PROFILE PORT
- K934640 — HMP DUAL POLYSULFONE PORT
Data sourced from openFDA. This site is unofficial and independent of the FDA.