Cleared Traditional

K121690 - ETCHONIA ZERONA ARMS (FDA 510(k) Clearance)

Aug 2012
Decision
77d
Days
Class 2
Risk

K121690 is an FDA 510(k) clearance for the ETCHONIA ZERONA ARMS. This device is classified as 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 August 23, 2012, 77 days after receiving the submission on June 7, 2012.

This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.5400. Non-invasive Reduction In Fat Layer For Body Contouring.

Submission Details

510(k) Number K121690 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 07, 2012
Decision Date August 23, 2012
Days to Decision 77 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