Cleared Traditional

Contour Light CL-100

K202955 · Contour Research, LLC · General & Plastic Surgery
May 2021
Decision
231d
Days
Class 2
Risk

About This 510(k) Submission

K202955 is an FDA 510(k) clearance for the Contour Light CL-100, a Fat Reducing Low Level Laser (Class II — Special Controls, product code OLI), submitted by Contour Research, LLC (Reno, US). The FDA issued a Cleared decision on May 19, 2021, 231 days after receiving the submission on September 30, 2020. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.5400.

Submission Details

510(k) Number K202955 FDA.gov
FDA Decision Cleared SESE
Date Received September 30, 2020
Decision Date May 19, 2021
Days to Decision 231 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