K-number	K062114
Device name	CERULOPLASMIN, MODEL 2055953
Applicant	Roche Diagnostics Corp.
Product code	CHN
Device class	Class II
Decision date	Jan 31, 2007
Decision	Substantially Equivalent
Regulation	866.5210

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View the full FDA submission: accessdata.fda.gov

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CERULOPLASMIN, MODEL 2055953

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