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DIRECTIGEN 1-2-3(TM) HCG TEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913122
510(k) Type
Traditional
Applicant
QUIDEL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/1991
Days to Decision
32 days
Submission Type
Summary

DIRECTIGEN 1-2-3(TM) HCG TEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913122
510(k) Type
Traditional
Applicant
QUIDEL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/1991
Days to Decision
32 days
Submission Type
Summary