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CLINIQA LIQUID QC BILIRUBIN CONTROLS LEVELS 1, 2 & 3; CLINIQA LINICAL BILIRUBIN CALIBRATION VERIFIERS LEVELS A-E

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052679
510(k) Type
Traditional
Applicant
CLINIQA CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/2005
Days to Decision
51 days
Submission Type
Summary

CLINIQA LIQUID QC BILIRUBIN CONTROLS LEVELS 1, 2 & 3; CLINIQA LINICAL BILIRUBIN CALIBRATION VERIFIERS LEVELS A-E

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052679
510(k) Type
Traditional
Applicant
CLINIQA CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/2005
Days to Decision
51 days
Submission Type
Summary