Erchonia EVRL— 510(k) K251843
Substantially EquivalentErchonia Corporation
FDA 510(k) clearance K251843 for Erchonia EVRL, Substantially Equivalent on 2025-09-12. Applicant: Erchonia Corporation. Device class: 2.
Clearance details
- Applicant
- Erchonia Corporation
- 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
- Fountain Inn, SC, US
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More clearances from Erchonia Corporation
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.