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FDA 510(k)

Slimming Treatment Device

K-Number: K161892 · 2017-03-02

ApplicantBeijing Honkon Technologies Co., Ltd.
Decision Date2017-03-02
Product CodeNUV
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Slimming Treatment Device is the device name listed in this FDA 510(k) record. The listed applicant is Beijing Honkon Technologies Co., Ltd.. It received FDA 510(k) clearance on 2017-03-02 under 510(k) 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. The listed applicant is Beijing Honkon Technologies Co., Ltd.. The 510(k) number is K161892.

When did Slimming Treatment Device receive FDA 510(k) clearance?

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

Who is the listed applicant for Slimming Treatment Device?

The FDA 510(k) record lists Beijing Honkon Technologies Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Slimming Treatment Device?

The FDA product code for Slimming Treatment Device is NUV.

Related Devices (Code: NUV)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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

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