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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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