FDA 510(k) Application Details - K071094

Device Classification Name	System, Gastrointestinal Motility (Electrical)   More FDA Info for this Device
510(K) Number	K071094
Device Name	System, Gastrointestinal Motility (Electrical)
Applicant	MEDICAL MEASUREMENT SYSTEMS,B.V. COLOSSEUM 25 ENSCHEDE 7521 PV NL Other 510(k) Applications for this Company
Contact	KARIN OGINK-SOMHORST Other 510(k) Applications for this Contact
Regulation Number	876.1725   More FDA Info for this Regulation Number
Classification Product Code	FFX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/18/2007
Decision Date	08/13/2007
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review