FDA 510(k)

Endo Motor

Número K: K222548 · 2023-04-26

RequerenteShenzhen Perfect Medical Instruments Co., Ltd.

Data da decisão2023-04-26

Código do produtoEKX

Comité consultivoDE

DecisãoSubstantially Equivalent

Resumo do dispositivo

Endo Motor is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Perfect Medical Instruments Co., Ltd.. It received FDA 510(k) clearance on 2023-04-26 under 510(k) number K222548. The device is classified under product code EKX. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Endo Motor?

Endo Motor is a medical device that received FDA 510(k) clearance on 2023-04-26. The listed applicant is Shenzhen Perfect Medical Instruments Co., Ltd.. The 510(k) number is K222548.

When did Endo Motor receive FDA 510(k) clearance?

Endo Motor received FDA 510(k) clearance on 2023-04-26, under 510(k) number K222548.

Who is the listed applicant for Endo Motor?

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

What is the FDA product code for Endo Motor?

The FDA product code for Endo Motor is EKX.

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