Horizon Medical Products, Inc.
FDA 510(k) medical device clearances.
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.