Cleared Traditional

K232795 - Led Mask Platinum Exclusive MD (FDA 510(k) Clearance)

Dec 2023
Decision
86d
Days
Class 2
Risk

K232795 is an FDA 510(k) clearance for the Led Mask Platinum Exclusive MD. This device is classified as a Light Based Over The Counter Wrinkle Reduction (Class II - Special Controls, product code OHS).

Submitted by Stg24 Co., Ltd. (Incheon, KR). The FDA issued a Cleared decision on December 7, 2023, 86 days after receiving the submission on September 12, 2023.

This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4810. Use Of Light Based Treatment To Reduce Wrinkles On The Body In General Or Specific Anatomical Locations Depending On The Information Provided..

Submission Details

510(k) Number K232795 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 12, 2023
Decision Date December 07, 2023
Days to Decision 86 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code OHS - Light Based Over The Counter Wrinkle Reduction
Device Class Class II - Special Controls
CFR Regulation 21 CFR 878.4810
Definition Use Of Light Based Treatment To Reduce Wrinkles On The Body In General Or Specific Anatomical Locations Depending On The Information Provided.

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