FDA 510(k) Application Details - K972825

Device Classification Name	Catheter, Biliary, Diagnostic   More FDA Info for this Device
510(K) Number	K972825
Device Name	Catheter, Biliary, Diagnostic
Applicant	CORDIS CORP. 14201 N.W. 60TH AVE. MIAMI LAKES, FL 33014 US Other 510(k) Applications for this Company
Contact	MIRJAM BARBOZA 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	07/09/1997
Decision Date	10/07/1997
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