FDA 510(k) Application Details - K023906

Device Classification Name	Stimulator, Electrical, Non-Implantable, For Incontinence   More FDA Info for this Device
510(K) Number	K023906
Device Name	Stimulator, Electrical, Non-Implantable, For Incontinence
Applicant	THE PROMETHEUS GROUP 1 WASHINGTON ST., SUITE 303 DOVER, NH 03820 US Other 510(k) Applications for this Company
Contact	HEATHER MAGOON Other 510(k) Applications for this Contact
Regulation Number	876.5320   More FDA Info for this Regulation Number
Classification Product Code	KPI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/22/2002
Decision Date	02/19/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review