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cobas c513 Analyzer, cobas c13 Tina-quant HbA1cDx Gen.3 Assay

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160571
510(k) Type
Traditional
Applicant
Roche Diagnostics Operations (Rdo)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/19/2016
Days to Decision
294 days
Submission Type
Summary

cobas c513 Analyzer, cobas c13 Tina-quant HbA1cDx Gen.3 Assay

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160571
510(k) Type
Traditional
Applicant
Roche Diagnostics Operations (Rdo)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/19/2016
Days to Decision
294 days
Submission Type
Summary