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IGE RADIOIMMUNOASSAY KIT

Page Type
Cleared 510(K)
510(k) Number
K831377
510(k) Type
Traditional
Applicant
AMERICAN DIAGNOSTIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/1983
Days to Decision
36 days

IGE RADIOIMMUNOASSAY KIT

Page Type
Cleared 510(K)
510(k) Number
K831377
510(k) Type
Traditional
Applicant
AMERICAN DIAGNOSTIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/1983
Days to Decision
36 days