meddevicedb.com FDA Device Reference

Ivory Glove Powder-Free Nitrile Examination Gloves

K213681 Class I Traditional
Decision Date
2022-04-21
Sponsor / Applicant
Ivory Gloves Sdn. Bhd.

Technical Specification

510(k) Submission ID K213681
Product Code LZA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2022-04-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Ivory Glove Powder-Free Nitrile Examination Gloves received FDA 510(k) clearance under submission number K213681, sponsored by Ivory Gloves 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 2022-04-21.

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.