K-number	K173341
Device name	Vivid E80, Vivid E90, Vivid E95
Applicant	GE Medical Systems
Product code	IYN
Device class	Class II
Decision date	Nov 2, 2017
Decision	Substantially Equivalent
Regulation	892.1550

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Source

View the full FDA submission: accessdata.fda.gov

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Vivid E80, Vivid E90, Vivid E95

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