meddevicedb.com FDA Device Reference

BUNNY ELECTRODE/STEALTH ELECTRODE PRE WIRED EEG

K911529 Class II Traditional
Decision Date
1992-11-09
Sponsor / Applicant
Lead-Lok, Inc.

Technical Specification

510(k) Submission ID K911529
Product Code DRX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2360
Decision Date 1992-11-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BUNNY ELECTRODE/STEALTH ELECTRODE PRE WIRED EEG received FDA 510(k) clearance under submission number K911529, sponsored by Lead-Lok, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1992-11-09.

Classification & Regulation

This clearance is catalogued under FDA product code DRX and 21 CFR 870.2360, within the Cardiovascular review panel as a Class II device.