K-number	K181934
Device name	Vivid T8, Vivid T9
Applicant	GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC
Product code	IYN
Device class	Class II
Decision date	Nov 6, 2018
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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