K-number	K200851
Device name	Vivid T8, Vivid T9
Applicant	GE Medical Systems Ultrasound and Primary Care Diagnostics
Product code	IYN
Device class	Class II
Decision date	Sep 9, 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 T8, Vivid T9

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