meddevicedb.com FDA Device Reference

RS ORANGE NITRILE MEDICAL EXAMINATION GLOVES (POWDER FREE)

K133193 Class I Traditional
Decision Date
2014-06-23
Sponsor / Applicant
Riverstone Resources Sdn Bhd

Technical Specification

510(k) Submission ID K133193
Product Code LZA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2014-06-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RS ORANGE NITRILE MEDICAL EXAMINATION GLOVES (POWDER FREE) received FDA 510(k) clearance under submission number K133193, sponsored by Riverstone Resources 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 2014-06-23.

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.