Cleared Traditional

CurrentBody Skin RF

K232424 · El Global Trade, Ltd. · General & Plastic Surgery
Mar 2024
Decision
208d
Days
Class 2
Risk

About This 510(k) Submission

K232424 is an FDA 510(k) clearance for the CurrentBody Skin RF, a Over-the-counter Radiofrequency Coagulation Device For Wrinkle Reduction (Class II — Special Controls, product code PAY), submitted by El Global Trade, Ltd. (Netanya, IL). The FDA issued a Cleared decision on March 6, 2024, 208 days after receiving the submission on August 11, 2023. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4420.

Submission Details

510(k) Number K232424 FDA.gov
FDA Decision Cleared SESE
Date Received August 11, 2023
Decision Date March 06, 2024
Days to Decision 208 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.