meddevicedb.com FDA Device Reference

STERILE NEOPRENE POWDER-FREE SURGICAL GLOVES WITH NITRILE COATING

K102500 Class I Traditional
Decision Date
2010-11-04
Sponsor / Applicant
Cardinal Health, Inc.

Technical Specification

510(k) Submission ID K102500
Product Code KGO
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4460
Decision Date 2010-11-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STERILE NEOPRENE POWDER-FREE SURGICAL GLOVES WITH NITRILE COATING received FDA 510(k) clearance under submission number K102500, sponsored by Cardinal Health, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2010-11-04.

Classification & Regulation

This clearance is catalogued under FDA product code KGO and 21 CFR 878.4460, within the General, Plastic Surgery review panel as a Class I device.