K-number	K083745
Device name	THE IC-PRO SYSTEM, MODEL VERSION 3.2
Applicant	Paieon, Inc.
Product code	IZI
Device class	Class II
Decision date	Feb 17, 2009
Decision	Substantially Equivalent
Regulation	892.1600

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View the full FDA submission: accessdata.fda.gov

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THE IC-PRO SYSTEM, MODEL VERSION 3.2

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