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FDA 510(k)

Nitrile Patient Examination Glove

K-Number: K222534 · 2022-11-23

ApplicantJiangxi Jiangxi Zhonghong Pulin Medical Products Co., Ltd.
Decision Date2022-11-23
Product CodeLZA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Nitrile Patient Examination Glove is a medical device manufactured by Jiangxi Jiangxi Zhonghong Pulin Medical Products Co., Ltd.. It received FDA 510(k) clearance on 2022-11-23 under approval number K222534. 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 Nitrile Patient Examination Glove?

Nitrile Patient Examination Glove is a medical device that received FDA 510(k) clearance on 2022-11-23. It is manufactured by Jiangxi Jiangxi Zhonghong Pulin Medical Products Co., Ltd.. The 510(k) number is K222534.

When was Nitrile Patient Examination Glove approved by the FDA?

Nitrile Patient Examination Glove received FDA 510(k) clearance on 2022-11-23, under approval number K222534.

What company makes Nitrile Patient Examination Glove?

Nitrile Patient Examination Glove is manufactured by Jiangxi Jiangxi Zhonghong Pulin Medical Products Co., Ltd..

What is the FDA product code for Nitrile Patient Examination Glove?

The FDA product code for Nitrile Patient Examination Glove is LZA.

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Related Devices (Code: LZA)

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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.

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