K-number	K093982
Device name	XELERIS 3 PROCESSING AND REVIEW WORKSTATION
Applicant	Ge Medical Systems F.I. Haifa
Product code	LLZ
Device class	Class II
Decision date	Jan 8, 2010
Decision	Substantially Equivalent
Regulation	892.2050

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Source

View the full FDA submission: accessdata.fda.gov

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XELERIS 3 PROCESSING AND REVIEW WORKSTATION

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