K-number	K202658
Device name	Vivid E80/ Vivid E90/ Vivid E95
Applicant	GE Medical Systems Ultrasound and Primary Care Diagnostics
Product code	IYN
Device class	Class II
Decision date	Mar 5, 2021
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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