K-number	K072640
Device name	IRISPEC,CA/CB/CC
Applicant	Iris Diagnostics
Product code	JJW
Device class	Class I
Decision date	Dec 21, 2007
Decision	Substantially Equivalent
Regulation	862.1660

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View the full FDA submission: accessdata.fda.gov

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IRISPEC,CA/CB/CC

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