meddevicedb.com FDA Device Reference

NITRILE EXAMINATION GLOVES, POWDER FREE, POLYMER COATED, PURPLE COLOR

K030245 Class I Traditional
Decision Date
2003-04-04
Sponsor / Applicant
Arista Latindo Industrial Ltd. P.T

Technical Specification

510(k) Submission ID K030245
Product Code LZA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2003-04-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NITRILE EXAMINATION GLOVES, POWDER FREE, POLYMER COATED, PURPLE COLOR received FDA 510(k) clearance under submission number K030245, sponsored by Arista Latindo Industrial Ltd. P.T. 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 2003-04-04.

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.