IPL + Diode Laser Machine— 510(k) K193328

Name: FDA 510(k) clearance K193328
Creator: U.S. Food and Drug Administration
Published: 2020-03-25

Substantially Equivalent

Beijing Globalipl Development Co., Ltd.

FDA 510(k) clearance K193328 for IPL + Diode Laser Machine, Substantially Equivalent on 2020-03-25. Applicant: Beijing Globalipl Development Co., Ltd.. Device class: 2.

Clearance details

Applicant: Beijing Globalipl Development Co., Ltd.
Product code: Code ONF
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 2019-12-02
Decision date: 2020-03-25
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.