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FDA 510(k)

Stronghold Group Nitrile Examination Glove, Powder Free

K-Number: K213859 · 2022-01-13

ApplicantStronghold Group, LLC
Decision Date2022-01-13
Product CodeLZA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Stronghold Group Nitrile Examination Glove, Powder Free is a medical device manufactured by Stronghold Group, LLC. It received FDA 510(k) clearance on 2022-01-13 under approval number K213859. 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 Stronghold Group Nitrile Examination Glove, Powder Free?

Stronghold Group Nitrile Examination Glove, Powder Free is a medical device that received FDA 510(k) clearance on 2022-01-13. It is manufactured by Stronghold Group, LLC. The 510(k) number is K213859.

When was Stronghold Group Nitrile Examination Glove, Powder Free approved by the FDA?

Stronghold Group Nitrile Examination Glove, Powder Free received FDA 510(k) clearance on 2022-01-13, under approval number K213859.

What company makes Stronghold Group Nitrile Examination Glove, Powder Free?

Stronghold Group Nitrile Examination Glove, Powder Free is manufactured by Stronghold Group, LLC.

What is the FDA product code for Stronghold Group Nitrile Examination Glove, Powder Free?

The FDA product code for Stronghold Group Nitrile Examination Glove, Powder Free 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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