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IMMULITE 2000 TSI Assay, IMMULITE 2000 TSI Calibration Verification Material

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K152061
510(k) Type
Traditional
Applicant
SIEMENS HEALTHCARE DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/3/2016
Days to Decision
223 days
Submission Type
Summary

IMMULITE 2000 TSI Assay, IMMULITE 2000 TSI Calibration Verification Material

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K152061
510(k) Type
Traditional
Applicant
SIEMENS HEALTHCARE DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/3/2016
Days to Decision
223 days
Submission Type
Summary