FDA 510(k) Applications Submitted by INTRATHERAPEUTICS, INC.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K990221	01/22/1999	INTRACOIL PERIPHERAL STENT	INTRATHERAPEUTICS, INC.
K980290	01/26/1998	ITI STENT	INTRATHERAPEUTICS, INC.
K981191	04/02/1998	ITI INTRAMAX GUIDE CATHETER 91, 78 AND 65	INTRATHERAPEUTICS, INC.
K011184	04/18/2001	INTRASTENT DOUBLESTRUT PARAMOUNT XS BILIARY ENDOPROSTHESIS	INTRATHERAPEUTICS, INC.
K992622	08/05/1999	INTRAMAX ITI GUIDE CATHETER	INTRATHERAPEUTICS, INC.
K003450	11/07/2000	INTRASTENT DOUBLESTRUT PARAMOUNT BILIARY ENDOPROSTHESIS	INTRATHERAPEUTICS, INC.
K003997	12/26/2000	INTRASTENT DOUBLESTRUT PARAMOUNT XS BILIARY ENDOPROSTHESIS	INTRATHERAPEUTICS, INC.
K990592	02/24/1999	INTRASTENT II	INTRATHERAPEUTICS, INC.
K001648	05/30/2000	INTRASTENT DOUBLESTRUT PARAMOUNT	INTRATHERAPEUTICS, INC.
K991929	06/08/1999	INTRASTENT	INTRATHERAPEUTICS, INC.
K992816	08/20/1999	MODIFICATION TO INTRASTENT	INTRATHERAPEUTICS, INC.
K993904	11/17/1999	INTRASTENT DOUBLESTRUT LD	INTRATHERAPEUTICS, INC.
K000864	03/17/2000	INTRASTENT DOUBLESTRUT XS STENT	INTRATHERAPEUTICS, INC.
K001257	04/19/2000	INTRACOIL STENT	INTRATHERAPEUTICS, INC.
K003040	09/29/2000	INTRASTENT PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY	INTRATHERAPEUTICS, INC.