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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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