meddevicedb.com FDA Device Reference

Orange Non Sterile Powder Free Nitrile Examination Gloves

K172642 Class I Traditional
Decision Date
2017-11-28
Sponsor / Applicant
Central Medicare Sdn Bhd

Technical Specification

510(k) Submission ID K172642
Product Code LZC
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2017-11-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Orange Non Sterile Powder Free Nitrile Examination Gloves received FDA 510(k) clearance under submission number K172642, sponsored by Central Medicare 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 2017-11-28.

Classification & Regulation

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