meddevicedb.com FDA Device Reference

Disposable Vinyl Glove

K202010 Class I Traditional
Decision Date
2020-10-16
Sponsor / Applicant
Better Health Medical Products Co., Ltd.

Technical Specification

510(k) Submission ID K202010
Product Code LYZ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2020-10-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Disposable Vinyl Glove received FDA 510(k) clearance under submission number K202010, sponsored by Better Health Medical Products 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 2020-10-16.

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.