Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Slimming Treatment Device

K-Number: K161892 · 2017-03-02

Decision Date2017-03-02
Product CodeNUV
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Slimming Treatment Device is a medical device manufactured by Beijing Honkon Technologies Co., Ltd.. It received FDA 510(k) clearance on 2017-03-02 under approval number K161892. The device is classified under product code NUV. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Slimming Treatment Device?

Slimming Treatment Device is a medical device that received FDA 510(k) clearance on 2017-03-02. It is manufactured by Beijing Honkon Technologies Co., Ltd.. The 510(k) number is K161892.

When was Slimming Treatment Device approved by the FDA?

Slimming Treatment Device received FDA 510(k) clearance on 2017-03-02, under approval number K161892.

What company makes Slimming Treatment Device?

Slimming Treatment Device is manufactured by Beijing Honkon Technologies Co., Ltd..

What is the FDA product code for Slimming Treatment Device?

The FDA product code for Slimming Treatment Device is NUV.

Related Clinical Trials

Related PubMed Literature

Related Devices (Code: NUV)

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.