K-number	K113758
Device name	VOLUSON E6/E8/E8EXPERT/E10
Applicant	GE Healthcare
Product code	IYE
Device class	Class II
Decision date	Jan 10, 2012
Decision	Substantially Equivalent
Regulation	892.5050

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Source

View the full FDA submission: accessdata.fda.gov

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VOLUSON E6/E8/E8EXPERT/E10

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