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AMPLIVUE C. DIFFICILE ASSAY

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123355
510(k) Type
Traditional
Applicant
Quidel Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/2012
Days to Decision
43 days
Submission Type
Summary

AMPLIVUE C. DIFFICILE ASSAY

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123355
510(k) Type
Traditional
Applicant
Quidel Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/2012
Days to Decision
43 days
Submission Type
Summary