meddevicedb.com FDA Device Reference

SURGEON POWDER-FREE GLOVES, LATEX, STERILE

K992679 Class I Traditional
Decision Date
1999-10-21
Sponsor / Applicant
Wear Safe Malaysia Sdn. Bhd.

Technical Specification

510(k) Submission ID K992679
Product Code KGO
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4460
Decision Date 1999-10-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SURGEON POWDER-FREE GLOVES, LATEX, STERILE received FDA 510(k) clearance under submission number K992679, sponsored by Wear Safe Malaysia 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 1999-10-21.

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.