Cleared Traditional

Zerona Z6 OTC

K162578 · Erchonia Corporation · General & Plastic Surgery
Dec 2016
Decision
92d
Days
Class 2
Risk

About This 510(k) Submission

K162578 is an FDA 510(k) clearance for the Zerona Z6 OTC, 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 December 16, 2016, 92 days after receiving the submission on September 15, 2016. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.5400.

Submission Details

510(k) Number K162578 FDA.gov
FDA Decision Cleared SESE
Date Received September 15, 2016
Decision Date December 16, 2016
Days to Decision 92 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