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

FDA 510(k) Number Submission Date Device Name Applicant
K973129 08/21/1997 DENVER ASCITES SHUNTS, DENVER ASCITES SHUNT PERCUTANEOUS ACCESS KITS DENVER BIOMATERIALS, INC.
K960456 01/30/1996 DENVER PARACENTESIS NEEDLE(60-1200) DENVER PARACENTESIS NEEDLE WITH DRAINAGE LINE(60-1100) DENVER PARACENTESIS TRAY DENVER BIOMATERIALS, INC.
K971753 05/12/1997 DENVER PLEURX PLEURAL CATHETER KIT, CATALOG NO. 50-7000, DENVER PLEURX HOME DRAINAGE KIT, CATALOG NO. 50-7500 DENVER BIOMATERIALS, INC.
K962814 07/19/1996 DENVER PLEURAL EFFUSION SHUNT WITH EXTERNAL PUMP CHAMBER DENVER BIOMATERIALS, INC.


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