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Q-Rejuvalight Pro Facewear (Model: P19-0023)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230042
510(k) Type
Traditional
Applicant
Light Tree Ventures Europe B.V.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
4/28/2023
Days to Decision
112 days
Submission Type
Summary

Q-Rejuvalight Pro Facewear (Model: P19-0023)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230042
510(k) Type
Traditional
Applicant
Light Tree Ventures Europe B.V.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
4/28/2023
Days to Decision
112 days
Submission Type
Summary