K-number	K011095
Device name	MODEL I0-3DUIMS 3D ULTRASOUND MANAGEMENT SYSTEM
Applicant	Iodp SA
Product code	IYO
Device class	Class II
Decision date	Jun 13, 2001
Decision	Substantially Equivalent
Regulation	892.1560

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View the full FDA submission: accessdata.fda.gov

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MODEL I0-3DUIMS 3D ULTRASOUND MANAGEMENT SYSTEM

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