FDA 510(k) Applications Submitted by IRIS INTERNATIONAL, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K093861 12/16/2009 IQ 20 SERIES ANALYZER, IQ 200 SERIES SYSTEM, NAD IQ LAMINA CRADLE IRIS INTERNATIONAL, INC.
K060280 02/02/2006 ICHEM 100 URINE CHEMISTRY ANALYZER IRIS INTERNATIONAL, INC.
K050235 02/01/2005 IQ 200 URINE ANALYZER BODY FLUIDS MODULE IRIS INTERNATIONAL, INC.


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