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POWDER-FREE RADIATION ATTENUATING NEOPRENE SURGICAL GLOVE (BLACK)

K022873 Class I Traditional
Decision Date
2003-03-21
Sponsor / Applicant
International Biomedical, Inc.

Technical Specification

510(k) Submission ID K022873
Product Code KGO
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4460
Decision Date 2003-03-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POWDER-FREE RADIATION ATTENUATING NEOPRENE SURGICAL GLOVE (BLACK) received FDA 510(k) clearance under submission number K022873, sponsored by International Biomedical, 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 2003-03-21.

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.