K-number	K022397
Device name	SIGNA 3.0T MAGNETIC RESONANCE SYSTEM
Applicant	GE Medical Systems
Product code	LNH
Device class	Class II
Decision date	Aug 22, 2002
Decision	Substantially Equivalent
Regulation	892.1000

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View the full FDA submission: accessdata.fda.gov

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SIGNA 3.0T MAGNETIC RESONANCE SYSTEM

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