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FDA 510(k) Applications Submitted by KAMIYA BIOMEDICAL COMPANY
FDA 510(k) Number
Submission Date
Device Name
Applicant
K121232
04/24/2012
K-ASSAY (R) FERRITIN REAGENT, K-ASSAY (R) FERRITIN CALIBRATOR
KAMIYA BIOMEDICAL COMPANY
K192727
09/27/2019
K-ASSAY (R) RF (Ver.2), K-ASSAY (R) RF Calibrator (Ver.2)
Kamiya Biomedical Company
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