FDA 510(k)

Slimming Treatment Device

Número K: K161892 · 2017-03-02

RequerenteBeijing Honkon Technologies Co., Ltd.

Data da decisão2017-03-02

Código do produtoNUV

Comité consultivoSU

DecisãoSubstantially Equivalent

Resumo do dispositivo

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.

Perguntas frequentes

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.

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