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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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