meddevicedb.com FDA Device Reference

VINYL EXAMINATION GLOVES POWDER FREE

K974777 Class I Traditional
Decision Date
1998-01-30
Sponsor / Applicant
Sun Flower Gloves Co., Ltd.

Technical Specification

510(k) Submission ID K974777
Product Code LYZ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 1998-01-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VINYL EXAMINATION GLOVES POWDER FREE received FDA 510(k) clearance under submission number K974777, sponsored by Sun Flower 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 1998-01-30.

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.