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FIAX RHEUMATOID FACTOR TEST KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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