meddevicedb.com FDA Device Reference

MIND MAP (20 CHANNEL EEG)

K860378 Class II Traditional
Decision Date
1986-08-12
Sponsor / Applicant
Mind Systems Corp.

Technical Specification

510(k) Submission ID K860378
Product Code OLT
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1400
Decision Date 1986-08-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MIND MAP (20 CHANNEL EEG) received FDA 510(k) clearance under submission number K860378, sponsored by Mind Systems Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1986-08-12.

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.