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Cold Sore Device (Model: QPZ-01)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222205
510(k) Type
Traditional
Applicant
Light Tree Ventures Europe B.V.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
10/7/2022
Days to Decision
74 days
Submission Type
Summary

Cold Sore Device (Model: QPZ-01)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222205
510(k) Type
Traditional
Applicant
Light Tree Ventures Europe B.V.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
10/7/2022
Days to Decision
74 days
Submission Type
Summary