FDA 510(k) Applications Submitted by Diode Art Engineering doing business as Air Relax

FDA 510(k) Number Submission Date Device Name Applicant
K211460 05/11/2021 Air Relax Plus Model AR-3.0 Diode Art Engineering doing business as Air Relax
K212491 08/09/2021 Air Relax Pro Model AR-4.0 Diode Art Engineering doing business as Air Relax


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