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LINICAL RF-CRP CALIBRATION VERIFIERS LEVELS A-E FOR BECKMAN COULTER SYNCHRON CX SYSTEMS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023661
510(k) Type
Traditional
Applicant
CLINIQA CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/6/2002
Days to Decision
36 days
Submission Type
Statement

LINICAL RF-CRP CALIBRATION VERIFIERS LEVELS A-E FOR BECKMAN COULTER SYNCHRON CX SYSTEMS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023661
510(k) Type
Traditional
Applicant
CLINIQA CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/6/2002
Days to Decision
36 days
Submission Type
Statement