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FDA 510(k)

MHD TENS

Número K: K190115 · 2019-06-19

RequerenteMinghuangda Electronic Co., Ltd.
Data da decisão2019-06-19
Código do produtoNUH
Comité consultivoNE
DecisãoSubstantially Equivalent

Resumo do dispositivo

MHD TENS is the device name listed in this FDA 510(k) record. The listed applicant is Minghuangda Electronic Co., Ltd.. It received FDA 510(k) clearance on 2019-06-19 under 510(k) number K190115. 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 MHD TENS?

MHD TENS is a medical device that received FDA 510(k) clearance on 2019-06-19. The listed applicant is Minghuangda Electronic Co., Ltd.. The 510(k) number is K190115.

When did MHD TENS receive FDA 510(k) clearance?

MHD TENS received FDA 510(k) clearance on 2019-06-19, under 510(k) number K190115.

Who is the listed applicant for MHD TENS?

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

What is the FDA product code for MHD TENS?

The FDA product code for MHD TENS is NUH.

Dispositivos Relacionados (Código: NUH)

Registros relacionados são pareados automaticamente usando nomes, códigos de produtos ou outros metadados. Um pareamento não estabelece um vínculo clínico, científico, corporativo ou regulatório verificado; revise as fontes oficiais vinculadas.

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Fonte oficial

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