Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Powder Free White, Black, and Purple Nitrile Examination Glove

K-Number: K231439 · 2023-08-11

Decision Date2023-08-11
Product CodeLZA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Powder Free White, Black, and Purple Nitrile Examination Glove is a medical device manufactured by S&S Glove Corporation. It received FDA 510(k) clearance on 2023-08-11 under approval number K231439. 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 Powder Free White, Black, and Purple Nitrile Examination Glove?

Powder Free White, Black, and Purple Nitrile Examination Glove is a medical device that received FDA 510(k) clearance on 2023-08-11. It is manufactured by S&S Glove Corporation. The 510(k) number is K231439.

When was Powder Free White, Black, and Purple Nitrile Examination Glove approved by the FDA?

Powder Free White, Black, and Purple Nitrile Examination Glove received FDA 510(k) clearance on 2023-08-11, under approval number K231439.

What company makes Powder Free White, Black, and Purple Nitrile Examination Glove?

Powder Free White, Black, and Purple Nitrile Examination Glove is manufactured by S&S Glove Corporation.

What is the FDA product code for Powder Free White, Black, and Purple Nitrile Examination Glove?

The FDA product code for Powder Free White, Black, and Purple Nitrile Examination Glove is LZA.

Related Clinical Trials

Other Devices by S&S Glove Corporation

Related Devices (Code: LZA)

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.