FDA 510(k) Application Details - K151471

Device Classification Name	Endoscopic Guidewire, Gastroenterology-Urology   More FDA Info for this Device
510(K) Number	K151471
Device Name	Endoscopic Guidewire, Gastroenterology-Urology
Applicant	Terumo Medical Corporation 265 Davidson Ave, Suite 320 Somerset, NJ 08873 US Other 510(k) Applications for this Company
Contact	Phebe Varghese Other 510(k) Applications for this Contact
Regulation Number	876.1500   More FDA Info for this Regulation Number
Classification Product Code	OCY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/01/2015
Decision Date	09/17/2015
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