meddevicedb.com FDA Device Reference

HI-TOUCH (TM) BRAND SURGICAL GLOVES

K874539 Class I Traditional
Decision Date
1987-12-14
Sponsor / Applicant
Apex Medical Technologies, Inc.

Technical Specification

510(k) Submission ID K874539
Product Code KGO
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4460
Decision Date 1987-12-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HI-TOUCH (TM) BRAND SURGICAL GLOVES received FDA 510(k) clearance under submission number K874539, sponsored by Apex Medical Technologies, 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 1987-12-14.

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.