meddevicedb.com FDA Device Reference

STERILE SURGICAL LATEX GLOVES

K883824 Class I Traditional
Decision Date
1988-10-13
Sponsor / Applicant
Intl. Trading Ventures, Inc.

Technical Specification

510(k) Submission ID K883824
Product Code KGO
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4460
Decision Date 1988-10-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STERILE SURGICAL LATEX GLOVES received FDA 510(k) clearance under submission number K883824, sponsored by Intl. Trading Ventures, 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 1988-10-13.

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.