Intense Pulsed Light Equipment— 510(k) K220385

Name: FDA 510(k) clearance K220385
Creator: U.S. Food and Drug Administration
Published: 2022-08-12

Substantially Equivalent

Beijing Globalipl Development Co., Ltd.

FDA 510(k) clearance K220385 for Intense Pulsed Light Equipment, Substantially Equivalent on 2022-08-12. 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: 2022-02-10
Decision date: 2022-08-12
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.