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IN VITRO FERRITIN RIA TEST

Page Type
Cleared 510(K)
510(k) Number
K770702
510(k) Type
Traditional
Applicant
CLINICAL ASSAYS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/1977
Days to Decision
60 days

IN VITRO FERRITIN RIA TEST

Page Type
Cleared 510(K)
510(k) Number
K770702
510(k) Type
Traditional
Applicant
CLINICAL ASSAYS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/1977
Days to Decision
60 days