K-number	K090346
Device name	ADVIA 2120/2120I BODY FLUIDS
Applicant	Siemens Healthcare Diagnostics
Product code	GKZ
Device class	Class II
Decision date	Jul 28, 2010
Decision	Substantially Equivalent
Regulation	864.5220

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View the full FDA submission: accessdata.fda.gov

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ADVIA 2120/2120I BODY FLUIDS

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