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QUICKVUE(TM) ONE-STEP HCG CONTROLS (POSIT/NEGATI)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K931761
510(k) Type
Traditional
Applicant
QUIDEL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/1993
Days to Decision
75 days
Submission Type
Summary

QUICKVUE(TM) ONE-STEP HCG CONTROLS (POSIT/NEGATI)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K931761
510(k) Type
Traditional
Applicant
QUIDEL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/1993
Days to Decision
75 days
Submission Type
Summary