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FDA 510(k) Applications Submitted by SHAWN KAPLAN
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
K091486
05/19/2009
K-ASSAY MICROALBUMIN AND K-ASSAY MICROALBUMIN CALIBRATOR
KAMIYA BIOMEDICAL CO.
K192727
09/27/2019
K-ASSAY (R) RF (Ver.2), K-ASSAY (R) RF Calibrator (Ver.2)
Kamiya Biomedical Company
K093137
10/05/2009
K-ASSAY CYSTATIN C REAGENT, CALIBRATOR AND CONTROL
KAMIYA BIOMEDICAL CO.
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