FDA 510(k) Applications Submitted by SIEMENS HELATHCARE DIAGNOSTICS INC.

FDA 510(k) Number Submission Date Device Name Applicant
K131275 05/03/2013 MICROSCAN DRIED GRAM-POSTIVE MIC/COMBO PANELS SIEMENS HELATHCARE DIAGNOSTICS INC.
K132391 08/01/2013 IMMULITE 2000 ANTI-TG AB CALIBRATION VERIFICATION MATERIAL, IMMULITE 2000 ANTI-TPO AB CALIBRATION VERIFICATIN MATERIAL SIEMENS HELATHCARE DIAGNOSTICS INC.


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