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IMMULITE 2000 CEA Calibration Verification Material

Page Type
Cleared 510(K)
510(k) Number
K143639
510(k) Type
Abbreviated
Applicant
Siemens Healthcare Diagnostics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/2015
Days to Decision
32 days
Submission Type
Summary

IMMULITE 2000 CEA Calibration Verification Material

Page Type
Cleared 510(K)
510(k) Number
K143639
510(k) Type
Abbreviated
Applicant
Siemens Healthcare Diagnostics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/2015
Days to Decision
32 days
Submission Type
Summary