FDA 510(k) Applications Submitted by BONNIE VIVIAN

FDA 510(k) Number	Submission Date	Device Name	Applicant
K011831	06/12/2001	MODIFICATION TO PLEURX PLEURAL CATHETER AND DRAINAGE KITS	DENVER BIOMEDICAL, INC.
K973129	08/21/1997	DENVER ASCITES SHUNTS, DENVER ASCITES SHUNT PERCUTANEOUS ACCESS KITS	DENVER BIOMATERIALS, INC.
K003451	11/07/2000	DENVER PAK W/ DOUBLE-VALVE ASCITES SHUNT,DENVER PAK W/ SINGLE-VALVED ASCITES SHUNT, DENVER PAK, DOUBLED-VALVED ASCITES T	DENVER BIOMEDICALS, INC.
K011862	06/14/2001	DENVER ASCITES SHUNT AND PERCUTANEOUS ACCESS KIT WITH ASCITIES SHUNT	DENVER BIOMEDICAL, INC.
K012235	07/17/2001	DENVER PLEURAL EFFUSION SHUNT AND DENVER PLEURAL EFFUSION SHUNT WITH EXTERNAL PUMP CHAMBER	DENVER BIOMEDICAL, INC.