K-number	K051449
Device name	GE VIVID 7 WITH OR WITHOUT SUFFIX
Applicant	GE Medical Systems
Product code	IYN
Device class	Class II
Decision date	Jun 16, 2005
Decision	Substantially Equivalent
Regulation	892.1550

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Source

View the full FDA submission: accessdata.fda.gov

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GE VIVID 7 WITH OR WITHOUT SUFFIX

Everything you need for a 510(k) submission. Nothing you don't.