meddevicedb.com FDA Device Reference

Black Pearl Nitrile Examination Glove

K232319 Class I Traditional
Decision Date
2024-04-22
Sponsor / Applicant
Ug Global Resources Sdn. Bhd.

Technical Specification

510(k) Submission ID K232319
Product Code LZA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2024-04-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Black Pearl Nitrile Examination Glove received FDA 510(k) clearance under submission number K232319, sponsored by Ug Global 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 2024-04-22.

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.