K-number	K103529
Device name	LIAISON XL ANALYZER MODEL 10050
Applicant	DiaSorin, Inc.
Product code	LOL
Device class	Class II
Decision date	Jan 21, 2011
Decision	Substantially Equivalent
Regulation	866.3310

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Source

View the full FDA submission: accessdata.fda.gov

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LIAISON XL ANALYZER MODEL 10050

Everything you need for a 510(k) submission. Nothing you don't.