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COMFIT POWDER FREE BLUE NITRILE EXAMINATION GLOVE, STERILE

K993313 Class I Traditional
Decision Date
1999-11-23
Sponsor / Applicant
Wrp Asia Pacific Sdn. Bhd.

Technical Specification

510(k) Submission ID K993313
Product Code LZA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 1999-11-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COMFIT POWDER FREE BLUE NITRILE EXAMINATION GLOVE, STERILE received FDA 510(k) clearance under submission number K993313, sponsored by Wrp Asia Pacific 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 1999-11-23.

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.