Cleared Traditional

Erchonia Zerona? VZ8

K243811 · Erchonia Corporation · General & Plastic Surgery
Jan 2025
Decision
30d
Days
Class 2
Risk

About This 510(k) Submission

K243811 is an FDA 510(k) clearance for the Erchonia Zerona? VZ8, a Fat Reducing Low Level Laser (Class II — Special Controls, product code OLI), submitted by Erchonia Corporation (Fountain Inn, US). The FDA issued a Cleared decision on January 10, 2025, 30 days after receiving the submission on December 11, 2024. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.5400.

Submission Details

510(k) Number K243811 FDA.gov
FDA Decision Cleared SESE
Date Received December 11, 2024
Decision Date January 10, 2025
Days to Decision 30 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code OLI — Fat Reducing Low Level Laser
Device Class Class II — Special Controls
CFR Regulation 21 CFR 878.5400
Definition Non-invasive Reduction In Fat Layer For Body Contouring

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