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EMG NAVIGATOR & EMG TRAVELER

K893130 Class II Traditional
Decision Date
1990-03-20
Sponsor / Applicant
Bio-Logic Systems Corp.

Technical Specification

510(k) Submission ID K893130
Product Code IKN
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.1375
Decision Date 1990-03-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EMG NAVIGATOR & EMG TRAVELER received FDA 510(k) clearance under submission number K893130, sponsored by Bio-Logic Systems Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 1990-03-20.

Classification & Regulation

This clearance is catalogued under FDA product code IKN and 21 CFR 890.1375, within the Physical Medicine review panel as a Class II device.