K-number	K082907
Device name	IC-PRO SYSTEM, VERSION 3.1.0.4
Applicant	Paieon, Inc.
Product code	IZI
Device class	Class II
Decision date	Nov 18, 2008
Decision	Substantially Equivalent
Regulation	892.1600

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View the full FDA submission: accessdata.fda.gov

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IC-PRO SYSTEM, VERSION 3.1.0.4

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