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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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