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EASYNET BODY POSITION MODULE

K040932 Class II Traditional
Decision Date
2004-07-01
Sponsor / Applicant
Cadwell Laboratories, Inc.

Technical Specification

510(k) Submission ID K040932
Product Code LEL
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5050
Decision Date 2004-07-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EASYNET BODY POSITION MODULE received FDA 510(k) clearance under submission number K040932, sponsored by Cadwell Laboratories, 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 2004-07-01.

Classification & Regulation

This clearance is catalogued under FDA product code LEL and 21 CFR 882.5050, within the Neurology review panel as a Class II device.