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TOPTOUCH /OTHER CLIENTS PRIVATE LABELING

K131826 Class I Traditional
Decision Date
2013-11-22
Sponsor / Applicant
Jiangsu Toptouch Glove Co., Ltd.

Technical Specification

510(k) Submission ID K131826
Product Code LYZ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2013-11-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TOPTOUCH /OTHER CLIENTS PRIVATE LABELING received FDA 510(k) clearance under submission number K131826, sponsored by Jiangsu Toptouch 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 2013-11-22.

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.