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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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