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AMPLIVUE C. DIFFICILE ASSAY

Page Type
Cleared 510(K)
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)
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