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)

Vinyl Patient Examination Gloves

K-Number: K211239 · 2021-07-17

Decision Date2021-07-17
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Vinyl Patient Examination Gloves is a medical device manufactured by Jiangxi Shengda Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2021-07-17 under approval number K211239. The device is classified under product code LYZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Vinyl Patient Examination Gloves?

Vinyl Patient Examination Gloves is a medical device that received FDA 510(k) clearance on 2021-07-17. It is manufactured by Jiangxi Shengda Medical Technology Co., Ltd.. The 510(k) number is K211239.

When was Vinyl Patient Examination Gloves approved by the FDA?

Vinyl Patient Examination Gloves received FDA 510(k) clearance on 2021-07-17, under approval number K211239.

What company makes Vinyl Patient Examination Gloves?

Vinyl Patient Examination Gloves is manufactured by Jiangxi Shengda Medical Technology Co., Ltd..

What is the FDA product code for Vinyl Patient Examination Gloves?

The FDA product code for Vinyl Patient Examination Gloves is LYZ.

Related Clinical Trials

Related Devices (Code: LYZ)

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.