FDA 510(k) Application Details - K082805

Device Classification Name	Stent, Ureteral   More FDA Info for this Device
510(K) Number	K082805
Device Name	Stent, Ureteral
Applicant	Q UROLOGICAL CORPORATION 1E MELVIN STREET P.O. BOX 793 NATICK, MA 01760 US Other 510(k) Applications for this Company
Contact	SCOTT M EPSTEIN Other 510(k) Applications for this Contact
Regulation Number	876.4620   More FDA Info for this Regulation Number
Classification Product Code	FAD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/24/2008
Decision Date	01/20/2010
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