FDA 510(k) Application Details - K090485

Device Classification Name	Dislodger, Stone, Biliary   More FDA Info for this Device
510(K) Number	K090485
Device Name	Dislodger, Stone, Biliary
Applicant	PERCUTANEOUS SYSTEMS, INCORPORATED 3260 HILLVIEW AVENUE PALO ALTO, CA 94304 US Other 510(k) Applications for this Company
Contact	THOMAS LAWSON Other 510(k) Applications for this Contact
Regulation Number	876.5010   More FDA Info for this Regulation Number
Classification Product Code	LQR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/25/2009
Decision Date	07/22/2009
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