FDA 510(k) Applications Submitted by DENVER BIOMEDICAL, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K011831 06/12/2001 MODIFICATION TO PLEURX PLEURAL CATHETER AND DRAINAGE KITS DENVER BIOMEDICAL, 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.
K052436 09/06/2005 PLEURX PLEURAL CATHETER KIT, MODEL 50-7000 DENVER BIOMEDICAL, INC.
K051711 06/27/2005 PLEURX PERITONEAL CATHETER KIT AND PLEURX DRAINAGE KITS DENVER BIOMEDICAL, INC.


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