Cleared Traditional

Narrowband UV Phototherapy Light Lamp (Model: HB-UPLL-01, HB-UPLL-02)

K223882 · Shenzhen Honpal Optoelectronic Technology Co., Ltd. · General & Plastic Surgery
Mar 2023
Decision
90d
Days
Class 2
Risk

About This 510(k) Submission

K223882 is an FDA 510(k) clearance for the Narrowband UV Phototherapy Light Lamp (Model: HB-UPLL-01, HB-UPLL-02), a Light, Ultraviolet, Dermatological (Class II — Special Controls, product code FTC), submitted by Shenzhen Honpal Optoelectronic Technology Co., Ltd. (Shenzhen, CN). The FDA issued a Cleared decision on March 27, 2023, 90 days after receiving the submission on December 27, 2022. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4630.

Submission Details

510(k) Number K223882 FDA.gov
FDA Decision Cleared SESE
Date Received December 27, 2022
Decision Date March 27, 2023
Days to Decision 90 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code FTC — Light, Ultraviolet, Dermatological
Device Class Class II — Special Controls
CFR Regulation 21 CFR 878.4630

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