K-number	K212491
Device name	Air Relax Pro Model AR-4.0
Applicant	Diode Art Engineering Doing Business AS Air Relax
Product code	IRP
Device class	Class II
Decision date	Sep 2, 2021
Decision	Substantially Equivalent
Regulation	890.5650

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Source

View the full FDA submission: accessdata.fda.gov

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Air Relax Pro Model AR-4.0

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