FDA 510(k)

Oral/Enteral Syringe with ENFit connector

Número K: K222772 · 2023-08-17

RequerenteAnhui Tiankang Medical Technology Co., Ltd.

Data da decisão2023-08-17

Código do produtoPNR

Comité consultivoGU

DecisãoSubstantially Equivalent

Resumo do dispositivo

Oral/Enteral Syringe with ENFit connector is the device name listed in this FDA 510(k) record. The listed applicant is Anhui Tiankang Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2023-08-17 under 510(k) number K222772. The device is classified under product code PNR. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Oral/Enteral Syringe with ENFit connector?

Oral/Enteral Syringe with ENFit connector is a medical device that received FDA 510(k) clearance on 2023-08-17. The listed applicant is Anhui Tiankang Medical Technology Co., Ltd.. The 510(k) number is K222772.

When did Oral/Enteral Syringe with ENFit connector receive FDA 510(k) clearance?

Oral/Enteral Syringe with ENFit connector received FDA 510(k) clearance on 2023-08-17, under 510(k) number K222772.

Who is the listed applicant for Oral/Enteral Syringe with ENFit connector?

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

What is the FDA product code for Oral/Enteral Syringe with ENFit connector?

The FDA product code for Oral/Enteral Syringe with ENFit connector is PNR.

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Dispositivos Relacionados (Código: PNR)

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Fonte oficial

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