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FDA 510(k) Applications Submitted by BONNIE B 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.
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