Denver Biomaterials, Inc.
Denver Biomaterials, Inc. holds FDA 510(k) medical device clearances, first cleared 1996, most recent 1998.
Top product codes for Denver Biomaterials, Inc.
Recent clearances by Denver Biomaterials, Inc.
- K973129 — DENVER ASCITES SHUNTS, DENVER ASCITES SHUNT PERCUTANEOUS ACCESS KITS
- K971753 — DENVER PLEURX PLEURAL CATHETER KIT, CATALOG NO. 50-7000, DENVER PLEURX HOME DRAINAGE KIT, CATALOG NO. 50-7500
- K962814 — DENVER PLEURAL EFFUSION SHUNT WITH EXTERNAL PUMP CHAMBER
- K960456 — DENVER PARACENTESIS NEEDLE(60-1200) DENVER PARACENTESIS NEEDLE WITH DRAINAGE LINE(60-1100) DENVER PARACENTESIS TRAY
Data sourced from openFDA. This site is unofficial and independent of the FDA.