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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