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ANTINUCLEAR ANTIBODY TEST KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K851369
510(k) Type
Traditional
Applicant
MODERN DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/1985
Days to Decision
40 days

ANTINUCLEAR ANTIBODY TEST KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K851369
510(k) Type
Traditional
Applicant
MODERN DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/1985
Days to Decision
40 days