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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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