Klox Biophotonic LumiHeal System— 510(k) DEN200005
UnknownKlox Technlogies, Inc.
FDA 510(k) clearance DEN200005 for Klox Biophotonic LumiHeal System, Unknown on 2021-12-03. Applicant: Klox Technlogies, Inc.. Device class: 2.
Clearance details
- Applicant
- Klox Technlogies, Inc.
- Product code
- Code QPE
- Device class
- Class 2
- Regulation
- 21 CFR 878.4880
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Laval, CA
Data sourced from openFDA. This site is unofficial and independent of the FDA.