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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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