meddevicedb.com FDA Device Reference

Vinyl Examination Gloves(Yellow)

K203666 Class I Traditional
Decision Date
2021-03-12
Sponsor / Applicant
Lutai Medical Technology Co., Ltd.

Technical Specification

510(k) Submission ID K203666
Product Code LYZ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2021-03-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Vinyl Examination Gloves(Yellow) received FDA 510(k) clearance under submission number K203666, sponsored by Lutai Medical 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 2021-03-12.

Classification & Regulation

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