K-number	K101203
Device name	TINA-QUANT ALBUMIN GEN 2
Applicant	Roche Diagnostics
Product code	DCF
Device class	Class II
Decision date	Sep 10, 2010
Decision	Substantially Equivalent
Regulation	866.5040

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View the full FDA submission: accessdata.fda.gov

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TINA-QUANT ALBUMIN GEN 2

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