meddevicedb.com FDA Device Reference

STERILE NITRILE POWDER-FREE EXAMINATION GLOVES

K010211 Class I Special
Decision Date
2001-02-15
Sponsor / Applicant
Allegiance Healthcare Corp.

Technical Specification

510(k) Submission ID K010211
Product Code LZC
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2001-02-15
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STERILE NITRILE POWDER-FREE EXAMINATION GLOVES received FDA 510(k) clearance under submission number K010211, sponsored by Allegiance Healthcare Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2001-02-15.

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.