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FDA 510(k)

Synguard Nitrile Exam Glove

K-Number: K220442 · 2022-05-12

ApplicantTianjin Aoshang Outdoor Equipment Co., Ltd.
Decision Date2022-05-12
Product CodeLZA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Synguard Nitrile Exam Glove is a medical device manufactured by Tianjin Aoshang Outdoor Equipment Co., Ltd.. It received FDA 510(k) clearance on 2022-05-12 under approval number K220442. 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 Synguard Nitrile Exam Glove?

Synguard Nitrile Exam Glove is a medical device that received FDA 510(k) clearance on 2022-05-12. It is manufactured by Tianjin Aoshang Outdoor Equipment Co., Ltd.. The 510(k) number is K220442.

When was Synguard Nitrile Exam Glove approved by the FDA?

Synguard Nitrile Exam Glove received FDA 510(k) clearance on 2022-05-12, under approval number K220442.

What company makes Synguard Nitrile Exam Glove?

Synguard Nitrile Exam Glove is manufactured by Tianjin Aoshang Outdoor Equipment Co., Ltd..

What is the FDA product code for Synguard Nitrile Exam Glove?

The FDA product code for Synguard Nitrile Exam Glove is LZA.

Other Devices by Tianjin Aoshang Outdoor Equipment Co., Ltd.

K210030Medical Surgical Mask

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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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