K-number	K093861
Device name	IQ 20 SERIES ANALYZER, IQ 200 SERIES SYSTEM, NAD IQ LAMINA CRADLE
Applicant	Iris International, Inc.
Product code	LKM
Device class	Class II
Decision date	Feb 5, 2010
Decision	Substantially Equivalent
Regulation	864.5200

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Source

View the full FDA submission: accessdata.fda.gov

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IQ 20 SERIES ANALYZER, IQ 200 SERIES SYSTEM, NAD IQ LAMINA CRADLE

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