meddevicedb.com FDA Device Reference

Glovmaster Nitrile Examination Glove Powder Free

K212914 Class I Traditional
Decision Date
2021-12-22
Sponsor / Applicant
Glovmaster Sdn. Bhd.

Technical Specification

510(k) Submission ID K212914
Product Code LZA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2021-12-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Glovmaster Nitrile Examination Glove Powder Free received FDA 510(k) clearance under submission number K212914, sponsored by Glovmaster 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 2021-12-22.

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.