Denver Biomaterials, Inc. is one of 9209 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
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
Denver Biomaterials, Inc. has 3 FDA 510(k) cleared medical devices. Based in Evergreen, US.
Historical record: 3 cleared submissions from 1996 to 1998. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Denver Biomaterials, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Denver Biomaterials, Inc.
4 devices
Cleared
Mar 17, 1998
DENVER ASCITES SHUNTS, DENVER ASCITES SHUNT PERCUTANEOUS ACCESS KITS
Gastroenterology & Urology
208d
Cleared
Jun 27, 1997
DENVER PLEURX PLEURAL CATHETER KIT, CATALOG NO. 50-7000, DENVER PLEURX HOME...
Anesthesiology
46d
Cleared
Apr 14, 1997
DENVER PLEURAL EFFUSION SHUNT WITH EXTERNAL PUMP CHAMBER
Gastroenterology & Urology
269d
Cleared
Apr 01, 1996
DENVER PARACENTESIS NEEDLE(60-1200) DENVER PARACENTESIS NEEDLE WITH DRAINAGE...
General & Plastic Surgery
62d