Intensity Pulsed Light Therapy System— 510(k) K233307

Name: FDA 510(k) clearance K233307
Creator: U.S. Food and Drug Administration
Published: 2024-03-15

Substantially Equivalent

Beijing Adss Development Co., Ltd.

FDA 510(k) clearance K233307 for Intensity Pulsed Light Therapy System, Substantially Equivalent on 2024-03-15. Applicant: Beijing Adss Development Co., Ltd.. Device class: 2.

Clearance details

Applicant: Beijing Adss Development Co., Ltd.
Product code: Code ONF
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 2023-09-29
Decision date: 2024-03-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Beijing, CN

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.