FDA 510(k) Applications Submitted by Jennifer Baird

FDA 510(k) Number Submission Date Device Name Applicant
K221203 04/26/2022 AHI System Fifth Eye Inc.
DEN200022 04/03/2020 Analytic for Hemodynamic Instability (AHI) Fifth Eye Inc.
K212219 07/16/2021 AHI System Fifth Eye Inc.


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