FDA 510(k)

Black Nitrile Powder Free Patient Examination Glove, Non Sterile

Número K: K233740 · 2024-02-13

Data da decisão2024-02-13

Código do produtoLZA

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

Black Nitrile Powder Free Patient Examination Glove, Non Sterile is the device name listed in this FDA 510(k) record. The listed applicant is W.A. Rubbermate Co., Ltd.. It received FDA 510(k) clearance on 2024-02-13 under 510(k) number K233740. The device is classified under product code LZA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Black Nitrile Powder Free Patient Examination Glove, Non Sterile?

Black Nitrile Powder Free Patient Examination Glove, Non Sterile is a medical device that received FDA 510(k) clearance on 2024-02-13. The listed applicant is W.A. Rubbermate Co., Ltd.. The 510(k) number is K233740.

When did Black Nitrile Powder Free Patient Examination Glove, Non Sterile receive FDA 510(k) clearance?

Black Nitrile Powder Free Patient Examination Glove, Non Sterile received FDA 510(k) clearance on 2024-02-13, under 510(k) number K233740.

Who is the listed applicant for Black Nitrile Powder Free Patient Examination Glove, Non Sterile?

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

What is the FDA product code for Black Nitrile Powder Free Patient Examination Glove, Non Sterile?

The FDA product code for Black Nitrile Powder Free Patient Examination Glove, Non Sterile is LZA.

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