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FIAX RHEUMATOID FACTOR TEST KIT

Page Type
Cleared 510(K)
510(k) Number
K812968
510(k) Type
Traditional
Applicant
INTL. DIAGNOSTIC TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/1981
Days to Decision
15 days

FIAX RHEUMATOID FACTOR TEST KIT

Page Type
Cleared 510(K)
510(k) Number
K812968
510(k) Type
Traditional
Applicant
INTL. DIAGNOSTIC TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/1981
Days to Decision
15 days