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T3 RADIOIMMUNOASSAY KIT

Page Type
Cleared 510(K)
510(k) Number
K802470
510(k) Type
Traditional
Applicant
AMERICAN DIAGNOSTIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/12/1980
Days to Decision
34 days

T3 RADIOIMMUNOASSAY KIT

Page Type
Cleared 510(K)
510(k) Number
K802470
510(k) Type
Traditional
Applicant
AMERICAN DIAGNOSTIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/12/1980
Days to Decision
34 days