meddevicedb.com FDA Device Reference

PATIENT EXAMINATION GLOVES (POWDER FREE)

K932116 Class I Traditional
Decision Date
1994-03-15
Sponsor / Applicant
Evergrade Healthcare Products Sdn Bhd

Technical Specification

510(k) Submission ID K932116
Product Code LYY
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 1994-03-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PATIENT EXAMINATION GLOVES (POWDER FREE) received FDA 510(k) clearance under submission number K932116, sponsored by Evergrade Healthcare Products 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 1994-03-15.

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.