meddevicedb.com FDA Device Reference

POWDER FREE STERILE NITRILE SURGICAL GLOVES (BLUE)

K062950 Class I Traditional
Decision Date
2006-12-21
Sponsor / Applicant
Hartalega Sdn Bhd

Technical Specification

510(k) Submission ID K062950
Product Code KGO
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4460
Decision Date 2006-12-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POWDER FREE STERILE NITRILE SURGICAL GLOVES (BLUE) received FDA 510(k) clearance under submission number K062950, sponsored by Hartalega 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 2006-12-21.

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.