Cardinal Health 303,Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardinal Health 303,Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Cardinal Health 303,Inc. has 4 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 4 cleared submissions from 2006 to 2009. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Cardinal Health 303,Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cardinal Health 303,Inc.
4 devices
Cleared
Jul 09, 2009
ALARIS PC UNIT, MODELS 8000 AND 8015
General Hospital
66d
Cleared
Dec 28, 2007
ALARIS SYSTEM WITH MMS, MODEL 8XXX
General Hospital
150d
Cleared
Feb 23, 2007
SIGNATURE EDITION INFUSION SYSTEM, MODELS 710X, 720X
General Hospital
25d
Cleared
Nov 28, 2006
SIGNATURE EDITION GOLD INFUSION SYSTEM, MODEL 7X3X
General Hospital
27d