FDA 510(k) Application Details - K101139

Device Classification Name	Unit, Electrosurgical, Endoscopic (With Or Without Accessories)   More FDA Info for this Device
510(K) Number	K101139
Device Name	Unit, Electrosurgical, Endoscopic (With Or Without Accessories)
Applicant	MEDTRONIC INC. 7000 CENTRAL AVENUE NE MINNEAPOLIS, MN 55432-3576 US Other 510(k) Applications for this Company
Contact	THOMAS REICHEL Other 510(k) Applications for this Contact
Regulation Number	876.4300   More FDA Info for this Regulation Number
Classification Product Code	KNS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/22/2010
Decision Date	05/21/2010
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review