Erchonia CLX (Model # CFL)— 510(k) K252574
Substantially EquivalentErchonia Corporation
FDA 510(k) clearance K252574 for Erchonia CLX (Model # CFL), Substantially Equivalent on 2025-12-15. Applicant: Erchonia Corporation. Device class: 2.
Clearance details
- Applicant
- Erchonia Corporation
- Product code
- Code OLI
- Device class
- Class 2
- Regulation
- 21 CFR 878.5400
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Fountain Inn, SC, US
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