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VINYL EXAMINATION GLOVES, PRE-POWDERED

K023145 Class I Traditional
Decision Date
2002-10-11
Sponsor / Applicant
Shandong Jiazhan Plastic Products Co., Ltd.

Technical Specification

510(k) Submission ID K023145
Product Code LYZ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2002-10-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VINYL EXAMINATION GLOVES, PRE-POWDERED received FDA 510(k) clearance under submission number K023145, sponsored by Shandong Jiazhan Plastic Products Co., 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 2002-10-11.

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.