K-number	K050235
Device name	IQ 200 URINE ANALYZER BODY FLUIDS MODULE
Applicant	Iris International, Inc.
Product code	GKL
Device class	Class II
Decision date	Mar 23, 2005
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 ANALYZER BODY FLUIDS MODULE

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