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DIRECTIGEN 1-2-3 PREGNANCY CONTROLS

Page Type
Cleared 510(K)
510(k) Number
K911664
510(k) Type
Traditional
Applicant
QUIDEL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/31/1991
Days to Decision
49 days

DIRECTIGEN 1-2-3 PREGNANCY CONTROLS

Page Type
Cleared 510(K)
510(k) Number
K911664
510(k) Type
Traditional
Applicant
QUIDEL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/31/1991
Days to Decision
49 days