FDA 510(k) Applications Submitted by HORIZON MEDICAL PRODUCTS, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K994196 |
12/13/1999 |
HORIZON MEDICAL PRODUCTS MICROPORT 2 PERIPHERAL ACCESS PORT SYSTEM |
HORIZON MEDICAL PRODUCTS, INC. |
| K013871 |
11/21/2001 |
LIFEGUARD SAFETY INFUSION SET |
HORIZON MEDICAL PRODUCTS, INC. |
| K010189 |
01/22/2001 |
VORTEX ACCESS SYSTEM |
HORIZON MEDICAL PRODUCTS, INC. |
| K010767 |
03/14/2001 |
LIFEPORT VTX ACCESS SYSTEM,MODEL VTX 7000 SERIES |
HORIZON MEDICAL PRODUCTS, INC. |
| K011916 |
06/20/2001 |
SUPER C HEMODIALYSIS/APHERESIS CHRONIC CATHETER, MODEL DC-36 SERIES, DC-40 SERIES, DC-45 SERIES |
HORIZON MEDICAL PRODUCTS, INC. |
| K031718 |
06/03/2003 |
LIFEVALVE CENTRAL VENOUS CATHTER |
HORIZON MEDICAL PRODUCTS, INC. |
| K032557 |
08/19/2003 |
TRIUMPH VTX WITH LIFEVALVE CATHETER |
HORIZON MEDICAL PRODUCTS, INC. |
| K022905 |
09/03/2002 |
LIFEJET F16 HEMODIALYSIS/APHERESIS CHRONIC CATHETER |
HORIZON MEDICAL PRODUCTS, INC. |
| K032754 |
09/05/2003 |
VORTEX MP |
HORIZON MEDICAL PRODUCTS, INC. |
| K033473 |
11/03/2003 |
MODIFICATION TO VORTEX MP VASCULAR ACCESS PORT |
HORIZON MEDICAL PRODUCTS, INC. |
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