K-number	K122114
Device name	LOGIQ S7 EXPERT, LOGIQ S7 PRO
Applicant	GE Healthcare
Product code	IYN
Device class	Class II
Decision date	Oct 3, 2012
Decision	Substantially Equivalent
Regulation	892.1550

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Source

View the full FDA submission: accessdata.fda.gov

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LOGIQ S7 EXPERT, LOGIQ S7 PRO

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