Last synced on 25 January 2026 at 3:41 am

IMMULITE 2000 ANTI-TG AB CALIBRATION VERIFICATION MATERIAL, IMMULITE 2000 ANTI-TPO AB CALIBRATION VERIFICATIN MATERIAL

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K132391
510(k) Type
Abbreviated
Applicant
Siemens Helathcare Diagnostics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/20/2013
Days to Decision
50 days
Submission Type
Summary

IMMULITE 2000 ANTI-TG AB CALIBRATION VERIFICATION MATERIAL, IMMULITE 2000 ANTI-TPO AB CALIBRATION VERIFICATIN MATERIAL

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K132391
510(k) Type
Abbreviated
Applicant
Siemens Helathcare Diagnostics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/20/2013
Days to Decision
50 days
Submission Type
Summary