Slimming Treatment Device— 510(k) K161892

Name: FDA 510(k) clearance K161892
Creator: U.S. Food and Drug Administration
Published: 2017-03-02

Substantially Equivalent

Beijing Honkon Technologies Co., Ltd.

FDA 510(k) clearance K161892 for Slimming Treatment Device, Substantially Equivalent on 2017-03-02. Applicant: Beijing Honkon Technologies Co., Ltd.. Device class: 2.

Clearance details

Applicant: Beijing Honkon Technologies Co., Ltd.
Product code: Code NUV
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 2016-07-11
Decision date: 2017-03-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Beijing, CN

Download summary PDF View on FDA.gov ↗

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