meddevicedb.com FDA Device Reference

BIOCLEAN CHEMO ULTIMATE POWDER FREE POLYCHLOROPRENE EXAMINATION GLOVES

K081971 Class I Traditional
Decision Date
2008-12-23
Sponsor / Applicant
Nitritex (M) Sdn. Bhd.

Technical Specification

510(k) Submission ID K081971
Product Code LZC
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2008-12-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIOCLEAN CHEMO ULTIMATE POWDER FREE POLYCHLOROPRENE EXAMINATION GLOVES received FDA 510(k) clearance under submission number K081971, sponsored by Nitritex (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 2008-12-23.

Classification & Regulation

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