FDA 510(k)

Electrode Pad

Número K: K241512 · 2025-01-15

RequerenteShenzhen Deliduo Medical Technology Co.,Ltd

Data da decisão2025-01-15

Código do produtoGXY

Comité consultivoNE

DecisãoSubstantially Equivalent

Resumo do dispositivo

Electrode Pad is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Deliduo Medical Technology Co.,Ltd. It received FDA 510(k) clearance on 2025-01-15 under 510(k) number K241512. The device is classified under product code GXY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Electrode Pad?

Electrode Pad is a medical device that received FDA 510(k) clearance on 2025-01-15. The listed applicant is Shenzhen Deliduo Medical Technology Co.,Ltd. The 510(k) number is K241512.

When did Electrode Pad receive FDA 510(k) clearance?

Electrode Pad received FDA 510(k) clearance on 2025-01-15, under 510(k) number K241512.

Who is the listed applicant for Electrode Pad?

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

What is the FDA product code for Electrode Pad?

The FDA product code for Electrode Pad is GXY.

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