FDA 510(k)

Disposable Veress Needles

Número K: K232401 · 2023-12-14

RequerenteHangzhou Kangji Medical Instrument Co., Ltd.

Data da decisão2023-12-14

Código do produtoHIF

Comité consultivoOB

DecisãoSubstantially Equivalent

Resumo do dispositivo

Disposable Veress Needles is the device name listed in this FDA 510(k) record. The listed applicant is Hangzhou Kangji Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2023-12-14 under 510(k) number K232401. The device is classified under product code HIF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Disposable Veress Needles?

Disposable Veress Needles is a medical device that received FDA 510(k) clearance on 2023-12-14. The listed applicant is Hangzhou Kangji Medical Instrument Co., Ltd.. The 510(k) number is K232401.

When did Disposable Veress Needles receive FDA 510(k) clearance?

Disposable Veress Needles received FDA 510(k) clearance on 2023-12-14, under 510(k) number K232401.

Who is the listed applicant for Disposable Veress Needles?

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

What is the FDA product code for Disposable Veress Needles?

The FDA product code for Disposable Veress Needles is HIF.

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