meddevicedb.com FDA Device Reference

SMART - FIT, POWDERFREE NITRILE EXAMINATION GLOVES

K971665 Class I Traditional
Decision Date
1997-06-27
Sponsor / Applicant
Sj Medical Products (M) Sdn Bhd

Technical Specification

510(k) Submission ID K971665
Product Code LZA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 1997-06-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SMART - FIT, POWDERFREE NITRILE EXAMINATION GLOVES received FDA 510(k) clearance under submission number K971665, sponsored by Sj Medical Products (M) 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 1997-06-27.

Classification & Regulation

This clearance is catalogued under FDA product code LZA and 21 CFR 880.6250, within the General Hospital review panel as a Class I device.