meddevicedb.com FDA Device Reference

POLYMER COATED CHLORINATED POWDER-FREE LATEX EXAMINATION GLOVES

K954221 Class I Traditional
Decision Date
1996-05-03
Sponsor / Applicant
Hartalega Sdn Bhd

Technical Specification

510(k) Submission ID K954221
Product Code LYY
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 1996-05-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POLYMER COATED CHLORINATED POWDER-FREE LATEX EXAMINATION GLOVES received FDA 510(k) clearance under submission number K954221, sponsored by Hartalega 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 1996-05-03.

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.