FDA 510(k) Application Details - K041962

Device Classification Name	Catheter, Biliary, Diagnostic   More FDA Info for this Device
510(K) Number	K041962
Device Name	Catheter, Biliary, Diagnostic
Applicant	ABBOTT LABORATORIES 400 SAGINAW DR. REDWOOD CITY, CA 94063 US Other 510(k) Applications for this Company
Contact	JOANNA KUSKOWSKI 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	07/21/2004
Decision Date	10/01/2004
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