meddevicedb.com FDA Device Reference

ELECTROENCEPHALOMYOGRAPH

K810359 Class II Traditional
Decision Date
1981-03-13
Sponsor / Applicant
Thoracel Research Labs.

Technical Specification

510(k) Submission ID K810359
Product Code OLT
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1400
Decision Date 1981-03-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELECTROENCEPHALOMYOGRAPH received FDA 510(k) clearance under submission number K810359, sponsored by Thoracel Research Labs.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1981-03-13.

Classification & Regulation

This clearance is catalogued under FDA product code OLT and 21 CFR 882.1400, within the Neurology review panel as a Class II device.