K-number	K121232
Device name	K-ASSAY (R) FERRITIN REAGENT, K-ASSAY (R) FERRITIN CALIBRATOR
Applicant	Kamiya Biomedical Company
Product code	DBF
Device class	Class II
Decision date	May 24, 2012
Decision	Substantially Equivalent
Regulation	866.5340

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View the full FDA submission: accessdata.fda.gov

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K-ASSAY (R) FERRITIN REAGENT, K-ASSAY (R) FERRITIN CALIBRATOR

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