K-number	K052897
Device name	GE DEFINIUM AMX 700, MODEL AMX 700
Applicant	General Electric Medical Systems
Product code	IZL
Device class	Class II
Decision date	Nov 8, 2005
Decision	Substantially Equivalent
Regulation	892.1720

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View the full FDA submission: accessdata.fda.gov

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GE DEFINIUM AMX 700, MODEL AMX 700

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