meddevicedb.com FDA Device Reference

EP-4 CLINICAL STIMULATOR

K040207 Class II Special
Decision Date
2004-02-27
Sponsor / Applicant
Ep Medsystems

Technical Specification

510(k) Submission ID K040207
Product Code JOQ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1750
Decision Date 2004-02-27
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EP-4 CLINICAL STIMULATOR received FDA 510(k) clearance under submission number K040207, sponsored by Ep Medsystems. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2004-02-27.

Classification & Regulation

This clearance is catalogued under FDA product code JOQ and 21 CFR 870.1750, within the Cardiovascular review panel as a Class II device.