meddevicedb.com FDA Device Reference

POWDERED VINYL PATIENT EXAMINIATION GLOVES, CLEAR (NON-COLORED)

K102976 Class I Traditional
Decision Date
2010-12-13
Sponsor / Applicant
Heze Juxinyuan Food Co., Ltd.

Technical Specification

510(k) Submission ID K102976
Product Code LYZ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2010-12-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POWDERED VINYL PATIENT EXAMINIATION GLOVES, CLEAR (NON-COLORED) received FDA 510(k) clearance under submission number K102976, sponsored by Heze Juxinyuan Food 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 2010-12-13.

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.