Cleared Traditional

STOP U (Packed Black USA), STOP U (Packed White USA)

K182774 · Pollogen, Ltd. · General & Plastic Surgery
Jun 2019
Decision
261d
Days
Class 2
Risk

About This 510(k) Submission

K182774 is an FDA 510(k) clearance for the STOP U (Packed Black USA), STOP U (Packed White USA), 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 June 19, 2019, 261 days after receiving the submission on October 1, 2018. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4420.

Submission Details

510(k) Number K182774 FDA.gov
FDA Decision Cleared SESE
Date Received October 01, 2018
Decision Date June 19, 2019
Days to Decision 261 days
Submission Type Traditional
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.