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MEDLINE NITRILE EXAM GLOVES W/ALOE -GREEN

K090568 Class I Traditional
Decision Date
2009-10-02
Sponsor / Applicant
Medline Industries, Inc.

Technical Specification

510(k) Submission ID K090568
Product Code LZA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2009-10-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDLINE NITRILE EXAM GLOVES W/ALOE -GREEN received FDA 510(k) clearance under submission number K090568, sponsored by Medline Industries, Inc.. 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 2009-10-02.

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.