Cold Sore Device (Model: QPZ-01)— 510(k) K222205
Substantially EquivalentLight Tree Ventures Europe B.V.
FDA 510(k) clearance K222205 for Cold Sore Device (Model: QPZ-01), Substantially Equivalent on 2022-10-07. Applicant: Light Tree Ventures Europe B.V.. Device class: 2.
Clearance details
- Applicant
- Light Tree Ventures Europe B.V.
- Product code
- Code OKJ
- Device class
- Class 2
- Regulation
- 21 CFR 878.4860
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Hague, NL
Recent devices under product code OKJ
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