Horizon Medical Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Horizon Medical Products, Inc. - FDA 510(k) Cleared Devices
16
Total
11
Cleared
0
Denied
Horizon Medical Products, Inc. has 11 FDA 510(k) cleared general hospital devices. Based in Atlanta, US.
Historical record: 11 cleared submissions from 1994 to 2003.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Horizon Medical Products, Inc.
16 devices
Cleared
Nov 18, 2003
MODIFICATION TO VORTEX MP VASCULAR ACCESS PORT
General Hospital
15d
Cleared
Sep 12, 2003
VORTEX MP
General Hospital
7d
Cleared
Sep 09, 2003
TRIUMPH VTX WITH LIFEVALVE CATHETER
General Hospital
21d
Cleared
Jul 02, 2003
LIFEVALVE CENTRAL VENOUS CATHTER
General Hospital
29d
Cleared
Dec 13, 2002
LIFEJET F16 HEMODIALYSIS/APHERESIS CHRONIC CATHETER
Gastroenterology & Urology
101d
Cleared
Mar 29, 2002
LIFEGUARD SAFETY INFUSION SET
General Hospital
128d
Cleared
Oct 31, 2001
SUPER C HEMODIALYSIS/APHERESIS CHRONIC CATHETER, MODEL DC-36 SERIES, DC-40...
Gastroenterology & Urology
133d
Cleared
Apr 10, 2001
LIFEPORT VTX ACCESS SYSTEM,MODEL VTX 7000 SERIES
General Hospital
27d
Cleared
Feb 12, 2001
VORTEX ACCESS SYSTEM
General Hospital
21d
Cleared
Feb 10, 2000
HORIZON MEDICAL PRODUCTS MICROPORT 2 PERIPHERAL ACCESS PORT SYSTEM
General Hospital
59d
Cleared
Aug 29, 1995
TRIUMPH-1 PORT
General Hospital
133d
Cleared
Feb 25, 1994
HMP POLYSULFONE PORT
General Hospital
192d
Cleared
Feb 25, 1994
HMP TITANIUM PORT
General Hospital
192d
Cleared
Feb 25, 1994
HMP DUAL TITANIUM PORT
General Hospital
163d
Cleared
Feb 25, 1994
HMP TITANIUM LOW PROFILE PORT
General Hospital
157d
Cleared
Feb 25, 1994
HMP DUAL POLYSULFONE PORT
General Hospital
150d