FDA 510(k)

DR-HO'S Electro Therapy Conductive Gel

Número K: K200402 · 2020-11-25

RequerenteGuangzhou Xinbo Electronic Co., Ltd.

Data da decisão2020-11-25

Código do produtoGYB

Comité consultivoNE

DecisãoSubstantially Equivalent

Resumo do dispositivo

DR-HO'S Electro Therapy Conductive Gel is the device name listed in this FDA 510(k) record. The listed applicant is Guangzhou Xinbo Electronic Co., Ltd.. It received FDA 510(k) clearance on 2020-11-25 under 510(k) number K200402. The device is classified under product code GYB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the DR-HO'S Electro Therapy Conductive Gel?

DR-HO'S Electro Therapy Conductive Gel is a medical device that received FDA 510(k) clearance on 2020-11-25. The listed applicant is Guangzhou Xinbo Electronic Co., Ltd.. The 510(k) number is K200402.

When did DR-HO'S Electro Therapy Conductive Gel receive FDA 510(k) clearance?

DR-HO'S Electro Therapy Conductive Gel received FDA 510(k) clearance on 2020-11-25, under 510(k) number K200402.

Who is the listed applicant for DR-HO'S Electro Therapy Conductive Gel?

The FDA 510(k) record lists Guangzhou Xinbo Electronic Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DR-HO'S Electro Therapy Conductive Gel?

The FDA product code for DR-HO'S Electro Therapy Conductive Gel is GYB.

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Outros registros que listam Guangzhou Xinbo Electronic Co., Ltd. como candidato(a)

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Fonte oficial

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