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VINYL EXAMINATION GLOVES STERILE POWEDERED

K020044 Class I Traditional
Decision Date
2002-02-26
Sponsor / Applicant
Primus Gloves Private , Ltd.

Technical Specification

510(k) Submission ID K020044
Product Code LYZ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2002-02-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VINYL EXAMINATION GLOVES STERILE POWEDERED received FDA 510(k) clearance under submission number K020044, sponsored by Primus Gloves Private , Ltd.. 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 2002-02-26.

Classification & Regulation

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