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OLYMPIC MEDICAL LECTROMED CEREBRAL FUNCTION MONITOR SYSTEM, MODEL 5330

K020335 Class II Traditional
Decision Date
2002-06-18
Sponsor / Applicant
Olympic Medical Corp.

Technical Specification

510(k) Submission ID K020335
Product Code OMC
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1400
Decision Date 2002-06-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OLYMPIC MEDICAL LECTROMED CEREBRAL FUNCTION MONITOR SYSTEM, MODEL 5330 received FDA 510(k) clearance under submission number K020335, sponsored by Olympic Medical 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 2002-06-18.

Classification & Regulation

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