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CDT CYTOTOXI TEST

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883560
510(k) Type
Traditional
Applicant
ADVANCED CLINICAL DIAGNOSTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/25/1988
Days to Decision
67 days

CDT CYTOTOXI TEST

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883560
510(k) Type
Traditional
Applicant
ADVANCED CLINICAL DIAGNOSTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/25/1988
Days to Decision
67 days