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LUSTRE 3XPRESS Light Beauty Therapy patches, model: PR6001, PR5001

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230720
510(k) Type
Traditional
Applicant
Light Tree Ventures Europe B.V.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
7/3/2023
Days to Decision
109 days
Submission Type
Summary

LUSTRE 3XPRESS Light Beauty Therapy patches, model: PR6001, PR5001

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230720
510(k) Type
Traditional
Applicant
Light Tree Ventures Europe B.V.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
7/3/2023
Days to Decision
109 days
Submission Type
Summary