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RADIOIMMUNOASSAY FOR HUMAN THYROID

Page Type
Cleared 510(K)
510(k) Number
K813392
510(k) Type
Traditional
Applicant
LEECO DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/1981
Days to Decision
19 days

RADIOIMMUNOASSAY FOR HUMAN THYROID

Page Type
Cleared 510(K)
510(k) Number
K813392
510(k) Type
Traditional
Applicant
LEECO DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/1981
Days to Decision
19 days