STOP U Model UXV Device

FDA 510(k) K203665 · Pollogen, Ltd.

Substantially Equivalent

510(k) numberK203665

Submission

Device name
STOP U Model UXV Device
Applicant
Pollogen, Ltd.
Tel Aviv, IL
Received
December 16, 2020
Decision date
February 25, 2021
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
PAY – Over-The-Counter Radiofrequency Coagulation Device For Wrinkle Reduction
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4420
Specialty
General, Plastic Surgery

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.

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K240616Faq™ (102)PAY · Traditional Foreo, Inc.07/15/2024SE
K233766Geneo X ElitePAY · Special Pollogen, Ltd.05/07/2024SE
K232424CurrentBody Skin RFPAY · Traditional El Global Trade, Ltd.03/06/2024SE
K230013Silk'n Titan AllwaysPAY · Traditional Silk'N Beauty , Ltd.08/30/2023SE
K220322Pollogen STOP U Model UXV DevicePAY · Traditional Pollogen, Ltd.05/04/2023SE
K222012Faq 101PAY · Traditional Foreo, Inc.04/05/2023SE
K182774STOP U (Packed Black USA), STOP U (Packed White USA)PAY · Traditional Pollogen, Ltd.06/19/2019SE
K170499sensiLiftPAY · Traditional El Global Trade, Ltd.06/15/2017SE

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K242227Geneo X ElitePAY · Traditional 10/12/2025SE
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K233766Geneo X ElitePAY · Special 05/07/2024SE
K232903Legend X PlatformGEI · Traditional 10/17/2023SE
K220322Pollogen STOP U Model UXV DevicePAY · Traditional 05/04/2023SE
K220124YandR System, VoluDerm Handpiece, VoluDerm TipsGEI · Special 02/17/2022SE
K200545Legend Pro DMANGX · Traditional 10/21/2021SE

Questions and answers

When was STOP U Model UXV Device cleared by the FDA?

STOP U Model UXV Device (K203665) received a 510(k) decision of Substantially Equivalent on February 25, 2021, 71 days after the submission was received.

What is the product code of K203665?

The FDA product code is PAY – Over-The-Counter Radiofrequency Coagulation Device For Wrinkle Reduction, a Class II (moderate risk) device regulated under 21 CFR 878.4420.