K-number	K200119
Device name	LOGIQ E10s
Applicant	GE Medical Systems Ultrasound and Primary Care Diagnostics
Product code	IYN
Device class	Class II
Decision date	Apr 1, 2020
Decision	Substantially Equivalent
Regulation	892.1550

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Source

View the full FDA submission: accessdata.fda.gov

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LOGIQ E10s

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