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EMG/NCV & EVOKED RESPONSE, DESIGN W/

K843253 Class II Traditional
Decision Date
1984-11-20
Sponsor / Applicant
Neurodiagnostics, Inc.

Technical Specification

510(k) Submission ID K843253
Product Code GWF
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1870
Decision Date 1984-11-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EMG/NCV & EVOKED RESPONSE, DESIGN W/ received FDA 510(k) clearance under submission number K843253, sponsored by Neurodiagnostics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1984-11-20.

Classification & Regulation

This clearance is catalogued under FDA product code GWF and 21 CFR 882.1870, within the Neurology review panel as a Class II device.