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POWDER-FREE VINYL PATIENT EXAMINATION GLOVES

K062522 Class I Traditional
Decision Date
2006-09-08
Sponsor / Applicant
Jiangsu Jaysun Glove Co., Ltd.

Technical Specification

510(k) Submission ID K062522
Product Code LYZ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2006-09-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POWDER-FREE VINYL PATIENT EXAMINATION GLOVES received FDA 510(k) clearance under submission number K062522, sponsored by Jiangsu Jaysun 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 2006-09-08.

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.