FDA 510(k) Application Details - K132672

Device Classification Name	Lithotriptor, Extracorporeal Shock-Wave,Urological   More FDA Info for this Device
510(K) Number	K132672
Device Name	Lithotriptor, Extracorporeal Shock-Wave,Urological
Applicant	DORNIER MEDTECH AMERICA 1155 ROBERTS BLVD. KENNESAW, GA 30144 US Other 510(k) Applications for this Company
Contact	JOHN HOFFER Other 510(k) Applications for this Contact
Regulation Number	876.5990   More FDA Info for this Regulation Number
Classification Product Code	LNS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/27/2013
Decision Date	09/23/2013
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review