Cardinal Health-Medical Products and Services is one of 16347 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardinal Health-Medical Products and Services - FDA 510(k) Cleared De...
Recent clearances: DURABLUE STERILIZATION WRAP, DURABLUE STERILIZATION WRAP, CARDINAL HEALTH DURABLUE STERILIZATION WRAP
6
Total
6
Cleared
0
Denied
Cardinal Health-Medical Products and Services has 6 FDA 510(k) cleared medical devices. Based in Waukegan, US.
Historical record: 6 cleared submissions from 1999 to 2013. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Cardinal Health-Medical Products and Services Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Underwriters Laboratories, Inc. and Cardinal Health,Medical Products and Services.
FDA 510(k) Regulatory Record - Cardinal Health-Medical Products and Services
6 devices
Cleared
Dec 13, 2013
DURABLUE STERILIZATION WRAP
General Hospital
163d
Cleared
Feb 28, 2013
DURABLUE STERILIZATION WRAP
General Hospital
129d
Cleared
Jun 01, 2012
CARDINAL HEALTH DURABLUE STERILIZATION WRAP
General Hospital
99d
Cleared
Apr 27, 2012
STERILE NEOPRENE POWDER-FREE SURGICAL GLOVES WITH NITRILE COATING
General Hospital
133d
Cleared
Sep 21, 2011
STERILE POLYISOPRENE POWDER-FREE BLUE SURGICAL GLOVES WITH NEU-THERA...
General Hospital
82d
Cleared
Jan 08, 1999
ULTRAFREE TEXTURED STERILE LATEX POWDER-FREE SURGICAL GLOVES
General Hospital
63d