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NITRILE POWDER-FREE MEDICAL EXAMINATION GLOVE (BROWN)

K012166 Class I Traditional
Decision Date
2001-08-01
Sponsor / Applicant
Best Manufacturing Company

Technical Specification

510(k) Submission ID K012166
Product Code LZA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2001-08-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NITRILE POWDER-FREE MEDICAL EXAMINATION GLOVE (BROWN) received FDA 510(k) clearance under submission number K012166, sponsored by Best Manufacturing Company. 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 2001-08-01.

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.