K-number	K132913
Device name	VOLUSON E6 / E8 / E8EXPERT / E8EXPERT LIMITED EDITION / E10
Applicant	GE Healthcare
Product code	IYN
Device class	Class II
Decision date	Nov 8, 2013
Decision	Substantially Equivalent
Regulation	892.1550

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Source

View the full FDA submission: accessdata.fda.gov

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VOLUSON E6 / E8 / E8EXPERT / E8EXPERT LIMITED EDITION / E10

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