FDA 510(k) Application Details - K991389

Device Classification Name	System, Gastrointestinal Motility (Electrical)   More FDA Info for this Device
510(K) Number	K991389
Device Name	System, Gastrointestinal Motility (Electrical)
Applicant	MEDTRONIC FUNCTIONAL DIAGNOSTICS A/S TONSBAKKEN 16-18 SKOVLUNDE COPENHAGEN DK-2740 DK Other 510(k) Applications for this Company
Contact	ANN-CHRISTINE JONSSON 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	04/21/1999
Decision Date	07/15/1999
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