Cardinal Health, Alaris Products is one of 16484 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardinal Health, Alaris Products - FDA 510(k) Cleared Devices
Recent clearances: SMARTSITE STOPCOCK, TEXIUM SYRINGE, SMARTSITE NEEDLE FREE VALVE ADMINISTRATION SETS
9
Total
9
Cleared
0
Denied
Cardinal Health, Alaris Products has 9 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 9 cleared submissions from 2005 to 2007. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Cardinal Health, Alaris Products Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Entela, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Cardinal Health, Alaris Products
9 devices
Cleared
Dec 14, 2007
SMARTSITE STOPCOCK
General Hospital
207d
Cleared
May 24, 2007
TEXIUM SYRINGE
General Hospital
35d
Cleared
Jul 26, 2006
SMARTSITE NEEDLE FREE VALVE ADMINISTRATION SETS
General Hospital
79d
Cleared
Jan 12, 2006
ALARIS SAFETY MALE LUER
General Hospital
76d
Cleared
Dec 23, 2005
SMARTSITE VENTED VIAL ACCESS DEVICE, MODEL TBD
General Hospital
81d
Cleared
Oct 20, 2005
ALARIS SYSTEM PC UNIT, MODEL 8001
General Hospital
122d
Cleared
Apr 01, 2005
BLOOD HAND PUMP ADMINISTRATION SET
General Hospital
73d
Cleared
Mar 25, 2005
SE INFUSION SYSTEM WITH MMS
General Hospital
87d
Cleared
Feb 16, 2005
TURBO TEMP TRIO
General Hospital
15d