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Air Relax Pro Model AR-4.0

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212491
510(k) Type
Traditional
Applicant
Diode Art Engineering doing business as Air Relax
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/2021
Days to Decision
24 days
Submission Type
Summary

Air Relax Pro Model AR-4.0

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212491
510(k) Type
Traditional
Applicant
Diode Art Engineering doing business as Air Relax
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/2021
Days to Decision
24 days
Submission Type
Summary