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POWDER FREE NITRILE EXAMINATION GLOVES, VIOLET COLOR

K011791 Class I Traditional
Decision Date
2001-08-01
Sponsor / Applicant
Latexx Partners Bhd.

Technical Specification

510(k) Submission ID K011791
Product Code LZA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2001-08-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POWDER FREE NITRILE EXAMINATION GLOVES, VIOLET COLOR received FDA 510(k) clearance under submission number K011791, sponsored by Latexx Partners 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 2001-08-01.

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.