Cleared Traditional

ZERONA 2.0 LASER

K123237 · Erchonia Corporation · General & Plastic Surgery
Jan 2013
Decision
101d
Days
Class 2
Risk

About This 510(k) Submission

K123237 is an FDA 510(k) clearance for the ZERONA 2.0 LASER, a Fat Reducing Low Level Laser (Class II — Special Controls, product code OLI), submitted by Erchonia Corporation (Littleton, US). The FDA issued a Cleared decision on January 25, 2013, 101 days after receiving the submission on October 16, 2012. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.5400.

Submission Details

510(k) Number K123237 FDA.gov
FDA Decision Cleared SESE
Date Received October 16, 2012
Decision Date January 25, 2013
Days to Decision 101 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Statement

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