meddevicedb.com FDA Device Reference

PATIENT EXAMINATION GLOVES (LATEX)

K891629 Class I Traditional
Decision Date
1989-07-31
Sponsor / Applicant
Union Rubber Gloves Co., Ltd.

Technical Specification

510(k) Submission ID K891629
Product Code LYY
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 1989-07-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PATIENT EXAMINATION GLOVES (LATEX) received FDA 510(k) clearance under submission number K891629, sponsored by Union Rubber Gloves 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 1989-07-31.

Classification & Regulation

This clearance is catalogued under FDA product code LYY and 21 CFR 880.6250, within the General Hospital review panel as a Class I device.