FDA 510(k) Application Details - K171336

Device Classification Name	Cystoscope And Accessories, Flexible/Rigid   More FDA Info for this Device
510(K) Number	K171336
Device Name	Cystoscope And Accessories, Flexible/Rigid
Applicant	Henke-Sass, Wolf GmbH Keltenstrasse 1 Tuttlingen 78532 DE Other 510(k) Applications for this Company
Contact	Anna Reifschneider Other 510(k) Applications for this Contact
Regulation Number	876.1500   More FDA Info for this Regulation Number
Classification Product Code	FAJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/08/2017
Decision Date	12/07/2017
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