K-number	K153037
Device name	LOGIQ V1/ LOGIQ V2
Applicant	GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC
Product code	IYN
Device class	Class II
Decision date	Jan 4, 2016
Decision	Substantially Equivalent
Regulation	892.1550

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Source

View the full FDA submission: accessdata.fda.gov

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LOGIQ V1/ LOGIQ V2

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