meddevicedb.com FDA Device Reference

SCIPOTEX POWDER FREE SURGICAL GLOVES (UNBEADED)

K943255 Class I Traditional
Decision Date
1995-03-07
Sponsor / Applicant
Wembley Rubber Products (M) Sdn Bhd

Technical Specification

510(k) Submission ID K943255
Product Code KGO
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4460
Decision Date 1995-03-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SCIPOTEX POWDER FREE SURGICAL GLOVES (UNBEADED) received FDA 510(k) clearance under submission number K943255, sponsored by Wembley Rubber Products (M) Sdn Bhd. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1995-03-07.

Classification & Regulation

This clearance is catalogued under FDA product code KGO and 21 CFR 878.4460, within the General, Plastic Surgery review panel as a Class I device.