FDA 510(k) Applications Submitted by Axess Vision Technology

FDA 510(k) Number Submission Date Device Name Applicant
K202180 08/04/2020 Broncoflex Agile; Product Reference: 20030001 , Broncoflex Vortex; Product Reference: 10030001, Screeni; Product Reference: 30030001 Axess Vision Technology
K212886 09/10/2021 Broncoflex Agile, Broncoflex Vortex, Screeni Axess Vision Technology


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