FDA 510(k) Application Details - K042686

Device Classification Name	Device, Discharge, Electrostatic (For Pain Relief)   More FDA Info for this Device
510(K) Number	K042686
Device Name	Device, Discharge, Electrostatic (For Pain Relief)
Applicant	ENERGEX SYSTEMS, INC. 719 A STREET NE WASHINGTON, DC 20002 US Other 510(k) Applications for this Company
Contact	TRISH LANDRY Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	NHH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/29/2004
Decision Date	06/16/2005
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	PM - Physical Medicine
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review