K-number	K103485
Device name	SENOGRAPH DS, SENOGRAPH ESSENSTIAL
Applicant	General Electric Company
Product code	MUE
Device class	Class II
Decision date	Oct 6, 2011
Decision	Substantially Equivalent
Regulation	892.1715

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View the full FDA submission: accessdata.fda.gov

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SENOGRAPH DS, SENOGRAPH ESSENSTIAL

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