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FDA 510(k) Applications Submitted by DENVER BIOMEDICALS, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
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.
K010642
03/05/2001
PLEURX PLEURAL CATHETER AND DRAINAGE KITS
DENVER BIOMEDICALS, INC.
K011020
04/04/2001
DENVER PLEURAL EFFUSION SHUNT WITH EXTERNAL PUMP CHAMBER
DENVER BIOMEDICALS, INC.
K051084
04/28/2005
DENVER PLEURX DRAINAGE KIT AND DENVER PLEURX VACUUM BOTTLE WITH DRAINAGE LINE
DENVER BIOMEDICALS, INC.
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