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POWDER FREE GLOVES

K935088 Class I Traditional
Decision Date
1994-04-05
Sponsor / Applicant
Avt Rubber Products , Ltd.

Technical Specification

510(k) Submission ID K935088
Product Code LYY
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 1994-04-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POWDER FREE GLOVES received FDA 510(k) clearance under submission number K935088, sponsored by Avt Rubber Products , 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 1994-04-05.

Classification & Regulation

This clearance is catalogued under FDA product code LYY and 21 CFR 880.6250, within the General Hospital review panel as a Class I device.