meddevicedb.com FDA Device Reference

Clear Vinyl Powder-free Patient Examination Gloves

K171317 Class I Traditional
Decision Date
2017-09-11
Sponsor / Applicant
Shandong Zhi Hong Medical Products, Co. , Ltd.

Technical Specification

510(k) Submission ID K171317
Product Code LYZ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2017-09-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Clear Vinyl Powder-free Patient Examination Gloves received FDA 510(k) clearance under submission number K171317, sponsored by Shandong Zhi Hong Medical Products, 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 2017-09-11.

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.