meddevicedb.com FDA Device Reference

POWDER FREE ELASTIC VINYL EXAMINATION GLOVES

K022604 Class I Traditional
Decision Date
2002-10-25
Sponsor / Applicant
Sun Flower Gloves Co., Ltd.

Technical Specification

510(k) Submission ID K022604
Product Code LYZ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2002-10-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POWDER FREE ELASTIC VINYL EXAMINATION GLOVES received FDA 510(k) clearance under submission number K022604, sponsored by Sun Flower Gloves 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 2002-10-25.

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.