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QUICKVUE SEMI-Q HCG-COMBO

Page Type
Cleared 510(K)
510(k) Number
K974052
510(k) Type
Traditional
Applicant
QUIDEL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/19/1997
Days to Decision
53 days
Submission Type
Summary

QUICKVUE SEMI-Q HCG-COMBO

Page Type
Cleared 510(K)
510(k) Number
K974052
510(k) Type
Traditional
Applicant
QUIDEL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/19/1997
Days to Decision
53 days
Submission Type
Summary