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IN VITRO FERRITIN RIA TEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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