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QUICKVUE ADVANCE PH AND AMINES GLL TEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040008
510(k) Type
Traditional
Applicant
QUIDEL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/2004
Days to Decision
118 days
Submission Type
Summary

QUICKVUE ADVANCE PH AND AMINES GLL TEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040008
510(k) Type
Traditional
Applicant
QUIDEL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/2004
Days to Decision
118 days
Submission Type
Summary