meddevicedb.com FDA Device Reference

SYNTHETIC VINYL EXAMINATION GLOVE POWDER FREE

K111857 Class I Traditional
Decision Date
2011-09-21
Sponsor / Applicant
Inmed Gloves Factory

Technical Specification

510(k) Submission ID K111857
Product Code LYZ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2011-09-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SYNTHETIC VINYL EXAMINATION GLOVE POWDER FREE received FDA 510(k) clearance under submission number K111857, sponsored by Inmed Gloves Factory. 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 2011-09-21.

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.