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FDA 510(k)

Black Nitrile Powder Free Patient Examination Glove, Non Sterile

K-Number: K233740 · 2024-02-13

ApplicantW.A. Rubbermate Co., Ltd.
Decision Date2024-02-13
Product CodeLZA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

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

Frequently Asked Questions

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. It is manufactured by W.A. Rubbermate Co., Ltd.. The 510(k) number is K233740.

When was Black Nitrile Powder Free Patient Examination Glove, Non Sterile approved by the FDA?

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

What company makes Black Nitrile Powder Free Patient Examination Glove, Non Sterile?

Black Nitrile Powder Free Patient Examination Glove, Non Sterile is manufactured by W.A. Rubbermate Co., Ltd..

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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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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