meddevicedb.com FDA Device Reference

SCIPOTEX POWDER FREE EXAM GLOVES (BEADED)

K942511 Class I Traditional
Decision Date
1995-02-03
Sponsor / Applicant
Wembley Rubber Products (M) Sdn Bhd

Technical Specification

510(k) Submission ID K942511
Product Code LYY
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 1995-02-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SCIPOTEX POWDER FREE EXAM GLOVES (BEADED) received FDA 510(k) clearance under submission number K942511, sponsored by Wembley Rubber Products (M) Sdn Bhd. 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 1995-02-03.

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.