meddevicedb.com FDA Device Reference

POWDER FREE LATEX EXAMINATION GLOVES, BLACK

K062709 Class I Traditional
Decision Date
2006-12-06
Sponsor / Applicant
Pt. Maja Agung Latexindo

Technical Specification

510(k) Submission ID K062709
Product Code LYY
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2006-12-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POWDER FREE LATEX EXAMINATION GLOVES, BLACK received FDA 510(k) clearance under submission number K062709, sponsored by Pt. Maja Agung Latexindo. 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 2006-12-06.

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.