FDA 510(k) Applications Submitted by Siemens Healthcare Diagnostics Products Ltd.

FDA 510(k) Number Submission Date Device Name Applicant
K202826 09/24/2020 IMMULITE« 2000 Cortisol Siemens Healthcare Diagnostics Products Ltd.
K203270 11/05/2020 IMMULITE/IMMULITE« 1000 Cortisol Siemens Healthcare Diagnostics Products Ltd.


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