FDA 510(k) Applications Submitted by ELENA S JUGO

FDA 510(k) Number	Submission Date	Device Name	Applicant
K971646	05/05/1997	4F NYLEX ANGIOGRAPHY CATHETER/5F NYLEX ANGIOGRAPHY CATHETER	CORDIS CORP.
K001843	06/19/2000	S.M.A.R.T. NITINOL STENT TRANSHEPATIC BILIARY SYSTEM	CORDIS CORP.
K152670	09/17/2015	DirectLink ICP Module, DirectLink ICP Extension Cable, Patient Monitor Interface Cables	Medos International SARL
K993646	10/29/1999	S.M.A.R.T. .018 NITINOL STENT TRANSHEPATIC BILIARY SYSTEM	CORDIS CORP.
K994068	12/02/1999	S.M.A.R.T. NITINOL STENT TRANSHEPATIC BILIARY SYSTEM	CORDIS CORP.
K970392	02/03/1997	CORDIS AVANTI+CATHETER SHEATH INTRODUCER SYSTEM	CORDIS CORP.
K970854	03/10/1997	5 FR AND 6 FR INFINITI ANGIOGRAPHIC CATHETER	CORDIS CORP.
K971608	05/01/1997	CORDIS BRITE TIP CATHETER SHEATH INTRODUCER SYSTEM	CORDIS CORP.
K041796	07/02/2004	PRECISE RX NITINOL STENT TRANSHEPATIC BILIARY SYSTEM	CORDIS CORPORATION
K003336	10/25/2000	MODIFICATION TO S.M.A.R.T NITINOL STENT TRANSHEPATIC BILIARY SYSTEM	CORDIS CORP.