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QUICKVUE ONE-STEP HCG-COMBO

Page Type
Cleared 510(K)
510(k) Number
K020801
510(k) Type
Traditional
Applicant
QUIDEL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/17/2002
Days to Decision
66 days
Submission Type
Summary

QUICKVUE ONE-STEP HCG-COMBO

Page Type
Cleared 510(K)
510(k) Number
K020801
510(k) Type
Traditional
Applicant
QUIDEL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/17/2002
Days to Decision
66 days
Submission Type
Summary