FDA 510(k) Application Details - K121112

Device Classification Name	Ureteroscope And Accessories, Flexible/Rigid   More FDA Info for this Device
510(K) Number	K121112
Device Name	Ureteroscope And Accessories, Flexible/Rigid
Applicant	Stryker Endoscopy 5900 OPTICAL CT. SAN JOSE, CA 95138 US Other 510(k) Applications for this Company
Contact	KEVIN POTGIETER, RAC Other 510(k) Applications for this Contact
Regulation Number	876.1500   More FDA Info for this Regulation Number
Classification Product Code	FGB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/12/2012
Decision Date	09/12/2012
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