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ANTISERUM TO HUMAN CERULOPLASMIN

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K790714
510(k) Type
Traditional
Applicant
KENT LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/1979
Days to Decision
126 days

ANTISERUM TO HUMAN CERULOPLASMIN

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K790714
510(k) Type
Traditional
Applicant
KENT LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/1979
Days to Decision
126 days