FDA 510(k) Application Details - K031769

Device Classification Name	Device, Iontophoresis, Other Uses   More FDA Info for this Device
510(K) Number	K031769
Device Name	Device, Iontophoresis, Other Uses
Applicant	EEMSO, INC. 1900 K STREET, NW WASHINGTON, DC 20006 US Other 510(k) Applications for this Company
Contact	LARRY R PILOT Other 510(k) Applications for this Contact
Regulation Number	890.5525   More FDA Info for this Regulation Number
Classification Product Code	EGJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/09/2003
Decision Date	10/14/2003
Decision	SN - Substantially Equivalent for Some Indications
Classification Advisory Committee	PM - Physical Medicine
Review Advisory Committee	PM - Physical Medicine
Statement / Summary / Purged Status
Type	Traditional
Reviewed By Third Party	N
Expedited Review