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FDA 510(k) Applications Submitted by Jennifer A. 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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