K-number	K091374
Device name	GE LOGIQ I/E & VIVID E COMPACT ULTRASOUND
Applicant	Ge Medical Systems China Co., Ltd.
Product code	IYO
Device class	Class II
Decision date	May 26, 2009
Decision	Substantially Equivalent
Regulation	892.1560

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View the full FDA submission: accessdata.fda.gov

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GE LOGIQ I/E & VIVID E COMPACT ULTRASOUND

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