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LINICAL HSCRP CALIBRATION VERIFIERS LEVELS A-E FOR THE DADE BN II NEPHELOMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022758
510(k) Type
Traditional
Applicant
CLINIQA CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/2002
Days to Decision
28 days
Submission Type
Statement

LINICAL HSCRP CALIBRATION VERIFIERS LEVELS A-E FOR THE DADE BN II NEPHELOMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022758
510(k) Type
Traditional
Applicant
CLINIQA CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/2002
Days to Decision
28 days
Submission Type
Statement