FDA 510(k) Application Details - K010684

Device Classification Name	Catheter, Biliary, Diagnostic   More FDA Info for this Device
510(K) Number	K010684
Device Name	Catheter, Biliary, Diagnostic
Applicant	GUIDANT CORP. 26531 YNEZ RD. TEMECULA, CA 92591-4630 US Other 510(k) Applications for this Company
Contact	BYRON LAMBERT Other 510(k) Applications for this Contact
Regulation Number	876.5010   More FDA Info for this Regulation Number
Classification Product Code	FGE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/08/2001
Decision Date	04/12/2001
Decision	SESU - SE - WITH LIMITATIONS
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