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FIAX CRP TEST KIT

Page Type
Cleared 510(K)
510(k) Number
K832054
510(k) Type
Traditional
Applicant
INTL. DIAGNOSTIC TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/26/1983
Days to Decision
60 days

FIAX CRP TEST KIT

Page Type
Cleared 510(K)
510(k) Number
K832054
510(k) Type
Traditional
Applicant
INTL. DIAGNOSTIC TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/26/1983
Days to Decision
60 days