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POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)

K100963 Class I Traditional
Decision Date
2010-08-06
Sponsor / Applicant
Hebei Shenzichen Plastic & Rubber Products Co., LT

Technical Specification

510(k) Submission ID K100963
Product Code LYZ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2010-08-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED) received FDA 510(k) clearance under submission number K100963, sponsored by Hebei Shenzichen Plastic & Rubber Products Co., LT. 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 2010-08-06.

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.