Cleared Traditional

Erchonia Emerald

K192544 · Erchonia Corporation · General & Plastic Surgery
Jan 2020
Decision
119d
Days
Class 2
Risk

About This 510(k) Submission

K192544 is an FDA 510(k) clearance for the Erchonia Emerald, a Fat Reducing Low Level Laser (Class II — Special Controls, product code OLI), submitted by Erchonia Corporation (Melbourne, US). The FDA issued a Cleared decision on January 13, 2020, 119 days after receiving the submission on September 16, 2019. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.5400.

Submission Details

510(k) Number K192544 FDA.gov
FDA Decision Cleared SESE
Date Received September 16, 2019
Decision Date January 13, 2020
Days to Decision 119 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