meddevicedb.com FDA Device Reference

POWDER FREE VINYL SYNTHETIC EXAMINATION GLOVES, WHITE COLOR (SENSI-PRO)

K040532 Class I Traditional
Decision Date
2004-03-23
Sponsor / Applicant
Zi BO Hong Wang Plastic & Rubber Products Co. , Ltd.

Technical Specification

510(k) Submission ID K040532
Product Code LYZ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2004-03-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POWDER FREE VINYL SYNTHETIC EXAMINATION GLOVES, WHITE COLOR (SENSI-PRO) received FDA 510(k) clearance under submission number K040532, sponsored by Zi BO Hong Wang Plastic & Rubber 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 2004-03-23.

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.