FDA 510(k) Application Details - K082536

Device Classification Name	Endoscopic Guidewire, Gastroenterology-Urology   More FDA Info for this Device
510(K) Number	K082536
Device Name	Endoscopic Guidewire, Gastroenterology-Urology
Applicant	COOK UROLOGICAL, INC. 1100 WEST MORGAN ST. SPENCER, IN 47460 US Other 510(k) Applications for this Company
Contact	CINDY FOOTE 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	09/02/2008
Decision Date	10/27/2008
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