K-number	K132062
Device name	ESIE APPS SUITE
Applicant	Siemens Medical Solutions USA, Inc.
Product code	LLZ
Device class	Class II
Decision date	Jul 23, 2013
Decision	Substantially Equivalent
Regulation	892.2050

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Source

View the full FDA submission: accessdata.fda.gov

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ESIE APPS SUITE

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