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K-ASSAY FERRITIN, K-ASSAY FERRITIN CALIBRATOR SET

Page Type
Cleared 510(K)
510(k) Number
K014293
510(k) Type
Traditional
Applicant
KAMIYA BIOMEDICAL CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/19/2002
Days to Decision
53 days
Submission Type
Statement

K-ASSAY FERRITIN, K-ASSAY FERRITIN CALIBRATOR SET

Page Type
Cleared 510(K)
510(k) Number
K014293
510(k) Type
Traditional
Applicant
KAMIYA BIOMEDICAL CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/19/2002
Days to Decision
53 days
Submission Type
Statement