meddevicedb.com FDA Device Reference

LATEX SURGICAL GLOVES

K864064 Class I Traditional
Decision Date
1986-10-30
Sponsor / Applicant
Futuremed Div. of Future Impex Corp.

Technical Specification

510(k) Submission ID K864064
Product Code KGO
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4460
Decision Date 1986-10-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LATEX SURGICAL GLOVES received FDA 510(k) clearance under submission number K864064, sponsored by Futuremed Div. of Future Impex Corp.. 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 1986-10-30.

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.