FDA 510(k)

Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff

Número K: K173044 · 2017-11-20

RequerenteNingbo Albert Novosino Co., Ltd.

Data da decisão2017-11-20

Código do produtoDXQ

Comité consultivoCV

DecisãoSubstantially Equivalent

Resumo do dispositivo

Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff is the device name listed in this FDA 510(k) record. The listed applicant is Ningbo Albert Novosino Co., Ltd.. It received FDA 510(k) clearance on 2017-11-20 under 510(k) number K173044. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff?

Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff is a medical device that received FDA 510(k) clearance on 2017-11-20. The listed applicant is Ningbo Albert Novosino Co., Ltd.. The 510(k) number is K173044.

When did Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff receive FDA 510(k) clearance?

Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff received FDA 510(k) clearance on 2017-11-20, under 510(k) number K173044.

Who is the listed applicant for Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff?

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

What is the FDA product code for Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff?

The FDA product code for Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff is DXQ.

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Dispositivos Relacionados (Código: DXQ)

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Fonte oficial

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