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FDA 510(k)

Glovmaster Nitrile Examination Glove Powder Free

K-Number: K212914 · 2021-12-22

Decision Date2021-12-22
Product CodeLZA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Glovmaster Nitrile Examination Glove Powder Free is a medical device manufactured by Glovmaster Sdn. Bhd.. It received FDA 510(k) clearance on 2021-12-22 under approval number K212914. 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 Glovmaster Nitrile Examination Glove Powder Free?

Glovmaster Nitrile Examination Glove Powder Free is a medical device that received FDA 510(k) clearance on 2021-12-22. It is manufactured by Glovmaster Sdn. Bhd.. The 510(k) number is K212914.

When was Glovmaster Nitrile Examination Glove Powder Free approved by the FDA?

Glovmaster Nitrile Examination Glove Powder Free received FDA 510(k) clearance on 2021-12-22, under approval number K212914.

What company makes Glovmaster Nitrile Examination Glove Powder Free?

Glovmaster Nitrile Examination Glove Powder Free is manufactured by Glovmaster Sdn. Bhd..

What is the FDA product code for Glovmaster Nitrile Examination Glove Powder Free?

The FDA product code for Glovmaster Nitrile Examination Glove Powder Free is LZA.

Related Clinical Trials

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.