meddevicedb.com FDA Device Reference

POWDER-FREE SYNTHETIC VINYL EXAM GLOVES WITH VITAMIN E COATING

K051683 Class I Traditional
Decision Date
2005-08-01
Sponsor / Applicant
Shen Wei (Usa), Inc.

Technical Specification

510(k) Submission ID K051683
Product Code LYZ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2005-08-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POWDER-FREE SYNTHETIC VINYL EXAM GLOVES WITH VITAMIN E COATING received FDA 510(k) clearance under submission number K051683, sponsored by Shen Wei (Usa), Inc.. 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 2005-08-01.

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.