K-number	K200158
Device name	LOGIQ E10
Applicant	GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC
Product code	IYN
Device class	Class II
Decision date	Apr 17, 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 E10

Everything you need for a 510(k) submission. Nothing you don't.