FDA 510(k)

Sterile and Non-Sterile Ultrasound Gels

Número K: K232957 · 2023-12-15

Data da decisão2023-12-15

Código do produtoMUI

Comité consultivoRA

DecisãoSubstantially Equivalent

Resumo do dispositivo

Sterile and Non-Sterile Ultrasound Gels is the device name listed in this FDA 510(k) record. The listed applicant is Jianerkang Medical Co., Ltd.. It received FDA 510(k) clearance on 2023-12-15 under 510(k) number K232957. The device is classified under product code MUI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Sterile and Non-Sterile Ultrasound Gels?

Sterile and Non-Sterile Ultrasound Gels is a medical device that received FDA 510(k) clearance on 2023-12-15. The listed applicant is Jianerkang Medical Co., Ltd.. The 510(k) number is K232957.

When did Sterile and Non-Sterile Ultrasound Gels receive FDA 510(k) clearance?

Sterile and Non-Sterile Ultrasound Gels received FDA 510(k) clearance on 2023-12-15, under 510(k) number K232957.

Who is the listed applicant for Sterile and Non-Sterile Ultrasound Gels?

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

What is the FDA product code for Sterile and Non-Sterile Ultrasound Gels?

The FDA product code for Sterile and Non-Sterile Ultrasound Gels is MUI.

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Dispositivos Relacionados (Código: MUI)

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Fonte oficial

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