meddevicedb.com FDA Device Reference

CONDUCTIVE GEL

K022006 Class II Traditional
Decision Date
2002-09-13
Sponsor / Applicant
The Dezac Group

Technical Specification

510(k) Submission ID K022006
Product Code GYB
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1275
Decision Date 2002-09-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CONDUCTIVE GEL received FDA 510(k) clearance under submission number K022006, sponsored by The Dezac Group. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2002-09-13.

Classification & Regulation

This clearance is catalogued under FDA product code GYB and 21 CFR 882.1275, within the Neurology review panel as a Class II device.