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FDA 510(k)

Black Nitrile Powder Free Patient Examination Glove, Non Sterile

K-Number: K222715 · 2022-12-03

Decision Date2022-12-03
Product CodeLZA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Black Nitrile Powder Free Patient Examination Glove, Non Sterile is a medical device manufactured by Safeskin Retailing (Hk) Limited. It received FDA 510(k) clearance on 2022-12-03 under approval number K222715. 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 2022-12-03. It is manufactured by Safeskin Retailing (Hk) Limited. The 510(k) number is K222715.

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 2022-12-03, under approval number K222715.

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

Black Nitrile Powder Free Patient Examination Glove, Non Sterile is manufactured by Safeskin Retailing (Hk) Limited.

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.

Related Clinical Trials

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Related Devices (Code: LZA)

Official Source

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