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V.D.T.-GONORRHEA TEST KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K840799
510(k) Type
Traditional
Applicant
M.G. LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/7/1984
Days to Decision
105 days

V.D.T.-GONORRHEA TEST KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K840799
510(k) Type
Traditional
Applicant
M.G. LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/7/1984
Days to Decision
105 days