FDA 510(k) Application Details - K042427

Device Classification Name	Lithotriptor, Extracorporeal Shock-Wave,Urological   More FDA Info for this Device
510(K) Number	K042427
Device Name	Lithotriptor, Extracorporeal Shock-Wave,Urological
Applicant	GENEMED, INC. 660 MAIN STREET SOUTH SUITE 7 WOODBURY, CT 06798 US Other 510(k) Applications for this Company
Contact	DAVID BALZER 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	09/08/2004
Decision Date	12/03/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review