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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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