K-number	K200743
Device name	Vivid E80/ Vivid E90/ Vivid E95
Applicant	Ge Medical Systems Ultrasound And
Product code	IYN
Device class	Class II
Decision date	Jul 23, 2020
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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