meddevicedb.com FDA Device Reference

VINYL EXAMINATION GLOVES

K893261 Class I Traditional
Decision Date
1989-07-14
Sponsor / Applicant
Clear Window Industrial, Ltd.

Technical Specification

510(k) Submission ID K893261
Product Code LYZ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 1989-07-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VINYL EXAMINATION GLOVES received FDA 510(k) clearance under submission number K893261, sponsored by Clear Window Industrial, 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 1989-07-14.

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.