Cleared Traditional

Erchonia Zerona Z-Bed

K220519 · Erchonia Corporation · General & Plastic Surgery
Mar 2022
Decision
29d
Days
Class 2
Risk

About This 510(k) Submission

K220519 is an FDA 510(k) clearance for the Erchonia Zerona Z-Bed, 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 March 24, 2022, 29 days after receiving the submission on February 23, 2022. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.5400.

Submission Details

510(k) Number K220519 FDA.gov
FDA Decision Cleared SESE
Date Received February 23, 2022
Decision Date March 24, 2022
Days to Decision 29 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