meddevicedb.com FDA Device Reference

Violet Nitrile Powder-Free Patient Examination Glove, Non Sterile

K220429 Class I Traditional
Decision Date
2022-05-13
Sponsor / Applicant
One Glove Industrial Sdn Bhd

Technical Specification

510(k) Submission ID K220429
Product Code LZA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2022-05-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Violet Nitrile Powder-Free Patient Examination Glove, Non Sterile received FDA 510(k) clearance under submission number K220429, sponsored by One Glove Industrial 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 2022-05-13.

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.