K-number	K091539
Device name	IQ 200 URINE ANALIZER BODY FLUIDS MODULE
Applicant	Iris Diagnostics
Product code	GKL
Device class	Class II
Decision date	Aug 31, 2010
Decision	Substantially Equivalent
Regulation	864.5200

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View the full FDA submission: accessdata.fda.gov

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IQ 200 URINE ANALIZER BODY FLUIDS MODULE

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