K-number	K960527
Device name	LOGIQ 1000 DIAGNOSTIC ULTRSOUND SYSTEM
Applicant	GE Medical Systems
Product code	IYN
Device class	Class II
Decision date	Sep 8, 1997
Decision	Substantially Equivalent
Regulation	892.1550

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View the full FDA submission: accessdata.fda.gov

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LOGIQ 1000 DIAGNOSTIC ULTRSOUND SYSTEM

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