Denver Biomaterials, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DENVER ASCITES SHUNTS, DENVER ASCITES SHUNT PERCUTANEOUS ACCESS KITS, DENVER PLEURX PLEURAL CATHETER KIT, CATALOG NO. 50-7000, DENVER PLEURX HOME DRAINAGE KIT, CATALOG NO. 50-7500, DENVER PLEURAL EFFUSION SHUNT WITH EXTERNAL PUMP CHAMBER
4
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Denver Biomaterials, Inc. Gastroenterology & Urology ✕
2 devices