meddevicedb.com FDA Device Reference

POWDER-FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR(NON-COLORED)

K062884 Class I Traditional
Decision Date
2006-11-09
Sponsor / Applicant
Suqian Green Glove Co., Ltd.

Technical Specification

510(k) Submission ID K062884
Product Code LYZ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2006-11-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POWDER-FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR(NON-COLORED) received FDA 510(k) clearance under submission number K062884, sponsored by Suqian Green 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 2006-11-09.

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.