meddevicedb.com FDA Device Reference

PEPPER GREEN MINT POWDERED LATEX EXAMINATION GLOVES

K993605 Class I Traditional
Decision Date
1999-12-20
Sponsor / Applicant
Top Glove Sdn. Bhd.

Technical Specification

510(k) Submission ID K993605
Product Code LYY
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 1999-12-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PEPPER GREEN MINT POWDERED LATEX EXAMINATION GLOVES received FDA 510(k) clearance under submission number K993605, sponsored by Top Glove 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 1999-12-20.

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.