meddevicedb.com FDA Device Reference

Disposable Nitrile Examination Gloves

K212833 Class I Traditional
Decision Date
2022-02-28
Sponsor / Applicant
Chifeng Huawei Medical Science&Technology Co., Ltd.

Technical Specification

510(k) Submission ID K212833
Product Code LZA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2022-02-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Disposable Nitrile Examination Gloves received FDA 510(k) clearance under submission number K212833, sponsored by Chifeng Huawei Medical Science&Technology Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2022-02-28.

Classification & Regulation

This clearance is catalogued under FDA product code LZA and 21 CFR 880.6250, within the General Hospital review panel as a Class I device.