meddevicedb.com FDA Device Reference

POWDER-FREE VINYL EXAM GLOVES

K052006 Class I Traditional
Decision Date
2005-08-03
Sponsor / Applicant
Baoding Guanzhong Glove Co., Ltd.

Technical Specification

510(k) Submission ID K052006
Product Code LYZ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2005-08-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POWDER-FREE VINYL EXAM GLOVES received FDA 510(k) clearance under submission number K052006, sponsored by Baoding Guanzhong Glove 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 2005-08-03.

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.