K-number	K102644
Device name	ADVIA 2120 WITH AUTOSLIDE SYSTEM, AND ADVIA 2120I
Applicant	Siemens Healthcare Diagnostics
Product code	GKZ
Device class	Class II
Decision date	Nov 23, 2011
Decision	Substantially Equivalent
Regulation	864.5220

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View the full FDA submission: accessdata.fda.gov

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ADVIA 2120 WITH AUTOSLIDE SYSTEM, AND ADVIA 2120I

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