Cleared Special

STOP U Model UXV Device

K203665 · Pollogen, Ltd. · General & Plastic Surgery
Feb 2021
Decision
71d
Days
Class 2
Risk

About This 510(k) Submission

K203665 is an FDA 510(k) clearance for the STOP U Model UXV Device, a Over-the-counter Radiofrequency Coagulation Device For Wrinkle Reduction (Class II — Special Controls, product code PAY), submitted by Pollogen, Ltd. (Tel Aviv, IL). The FDA issued a Cleared decision on February 25, 2021, 71 days after receiving the submission on December 16, 2020. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4420.

Submission Details

510(k) Number K203665 FDA.gov
FDA Decision Cleared SESE
Date Received December 16, 2020
Decision Date February 25, 2021
Days to Decision 71 days
Submission Type Special
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code PAY — Over-the-counter Radiofrequency Coagulation Device For Wrinkle Reduction
Device Class Class II — Special Controls
CFR Regulation 21 CFR 878.4420
Definition An Electrosurgical Device For Over-the-counter Aesthetic Use Is A Device Using Radiofrequency Energy To Produce Localized Heating Within Tissues For Non-invasive Aesthetic Use.