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POWDER FREE NITRILE (BLUE AND WHITE) EXAMINATION GLOVES

K081592 Class I Traditional
Decision Date
2008-12-03
Sponsor / Applicant
Quality Gallant Sdn. Bhd.

Technical Specification

510(k) Submission ID K081592
Product Code LZA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2008-12-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POWDER FREE NITRILE (BLUE AND WHITE) EXAMINATION GLOVES received FDA 510(k) clearance under submission number K081592, sponsored by Quality Gallant 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 2008-12-03.

Classification & Regulation

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