meddevicedb.com FDA Device Reference

EVER-MORE POWDER-FREE LATEX EXAMINATION GLOVES, BLUE COLOR

K023522 Class I Traditional
Decision Date
2002-11-29
Sponsor / Applicant
Ever-More Latex Products Sdn Bhd

Technical Specification

510(k) Submission ID K023522
Product Code LYY
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2002-11-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EVER-MORE POWDER-FREE LATEX EXAMINATION GLOVES, BLUE COLOR received FDA 510(k) clearance under submission number K023522, sponsored by Ever-More Latex Products Sdn Bhd. 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 2002-11-29.

Classification & Regulation

This clearance is catalogued under FDA product code LYY and 21 CFR 880.6250, within the General Hospital review panel as a Class I device.