FDA 510(k)

Single Use Suction-Evacuation Ureteral Access Sheath

Número K: K250128 · 2025-09-19

RequerenteAnhui Happiness Workshop Medical Instruments Co., Ltd.

Data da decisão2025-09-19

Código do produtoFED

Comité consultivoGU

DecisãoSubstantially Equivalent

Resumo do dispositivo

Single Use Suction-Evacuation Ureteral Access Sheath is the device name listed in this FDA 510(k) record. The listed applicant is Anhui Happiness Workshop Medical Instruments Co., Ltd.. It received FDA 510(k) clearance on 2025-09-19 under 510(k) number K250128. The device is classified under product code FED. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Single Use Suction-Evacuation Ureteral Access Sheath?

Single Use Suction-Evacuation Ureteral Access Sheath is a medical device that received FDA 510(k) clearance on 2025-09-19. The listed applicant is Anhui Happiness Workshop Medical Instruments Co., Ltd.. The 510(k) number is K250128.

When did Single Use Suction-Evacuation Ureteral Access Sheath receive FDA 510(k) clearance?

Single Use Suction-Evacuation Ureteral Access Sheath received FDA 510(k) clearance on 2025-09-19, under 510(k) number K250128.

Who is the listed applicant for Single Use Suction-Evacuation Ureteral Access Sheath?

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

What is the FDA product code for Single Use Suction-Evacuation Ureteral Access Sheath?

The FDA product code for Single Use Suction-Evacuation Ureteral Access Sheath is FED.

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Dispositivos Relacionados (Código: FED)

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