LUSTRE 3XPRESS Light Beauty Therapy patches, model: PR6001, PR5001— 510(k) K230720
Substantially EquivalentLight Tree Ventures Europe B.V.
FDA 510(k) clearance K230720 for LUSTRE 3XPRESS Light Beauty Therapy patches, model: PR6001, PR5001, Substantially Equivalent on 2023-07-03. Applicant: Light Tree Ventures Europe B.V.. Device class: 2.
Clearance details
- Applicant
- Light Tree Ventures Europe B.V.
- Product code
- Code OLP
- Device class
- Class 2
- Regulation
- 21 CFR 878.4810
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Hague, NL
Recent devices under product code OLP
view allMore clearances from Light Tree Ventures Europe B.V.
view allAdverse events under product code OLP
product code OLP- Other
- 1
- Total
- 1
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.