FDA 510(k) Applications for Medical Device Product Code "QNV"

FDA 510(k) Number Applicant Device Name Decision Date
K212219 Fifth Eye Inc. AHI System 12/03/2021
K221203 Fifth Eye Inc. AHI System 07/14/2022
DEN200022 Fifth Eye Inc. Analytic for Hemodynamic Instability (AHI) 03/01/2021


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