FDA 510(k) Applications Submitted by CARDINAL HEALTH, ALARIS PRODUCTS
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K050115 |
01/18/2005 |
BLOOD HAND PUMP ADMINISTRATION SET |
CARDINAL HEALTH, ALARIS PRODUCTS |
K050230 |
02/01/2005 |
TURBO TEMP TRIO |
CARDINAL HEALTH, ALARIS PRODUCTS |
K071108 |
04/19/2007 |
TEXIUM SYRINGE |
CARDINAL HEALTH, ALARIS PRODUCTS |
K061285 |
05/08/2006 |
SMARTSITE NEEDLE FREE VALVE ADMINISTRATION SETS |
CARDINAL HEALTH, ALARIS PRODUCTS |
K071400 |
05/21/2007 |
SMARTSITE STOPCOCK |
CARDINAL HEALTH, ALARIS PRODUCTS |
K051641 |
06/20/2005 |
ALARIS SYSTEM PC UNIT, MODEL 8001 |
CARDINAL HEALTH, ALARIS PRODUCTS |
K052790 |
10/03/2005 |
SMARTSITE VENTED VIAL ACCESS DEVICE, MODEL TBD |
CARDINAL HEALTH, ALARIS PRODUCTS |
K053049 |
10/28/2005 |
ALARIS SAFETY MALE LUER |
CARDINAL HEALTH, ALARIS PRODUCTS |
K043590 |
12/28/2004 |
SE INFUSION SYSTEM WITH MMS |
CARDINAL HEALTH, ALARIS PRODUCTS |
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