FDA 510(k)

Electronic stimulator

Número K: K200354 · 2020-06-29

RequerenteShenzhen Dongjilian Electronics Co., Ltd.

Data da decisão2020-06-29

Código do produtoNUH

Comité consultivoNE

DecisãoSubstantially Equivalent

Resumo do dispositivo

Electronic stimulator is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Dongjilian Electronics Co., Ltd.. It received FDA 510(k) clearance on 2020-06-29 under 510(k) number K200354. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Electronic stimulator?

Electronic stimulator is a medical device that received FDA 510(k) clearance on 2020-06-29. The listed applicant is Shenzhen Dongjilian Electronics Co., Ltd.. The 510(k) number is K200354.

When did Electronic stimulator receive FDA 510(k) clearance?

Electronic stimulator received FDA 510(k) clearance on 2020-06-29, under 510(k) number K200354.

Who is the listed applicant for Electronic stimulator?

The FDA 510(k) record lists Shenzhen Dongjilian Electronics Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Electronic stimulator?

The FDA product code for Electronic stimulator is NUH.

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Outros registros que listam Shenzhen Dongjilian Electronics Co., Ltd. como candidato(a)

K201694Dispositivo de Terapia de Compressão de Ar K193354Dispositivo de Terapia de Compressão de Ar

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Fonte oficial

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