meddevicedb.com FDA Device Reference

NITRILE POWDER FREE PATIENT EXAMINATION GLOVES

K110185 Class I Traditional
Decision Date
2011-04-04
Sponsor / Applicant
Tangshan Baojie Glove Co., Ltd.

Technical Specification

510(k) Submission ID K110185
Product Code LZA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2011-04-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NITRILE POWDER FREE PATIENT EXAMINATION GLOVES received FDA 510(k) clearance under submission number K110185, sponsored by Tangshan Baojie Glove 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 2011-04-04.

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.