Codman & Shurtleff, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CERENOVUS Large Bore Catheter, CERENOVUS Large Bore Catheter, CereLink ICP Sensor Basic Kit, CereLink ICP Sensor Metal Skull Bolt Kit, CereLink ICP Sensor Plastic Skull Bolt Kit, CereLink ICP Sensor Ventricular Catheter Kit
152
Total
151
Cleared
0
Denied
FDA 510(k) Regulatory Record - Codman & Shurtleff, Inc. General Hospital ✕
4 devices
Cleared
Apr 16, 2012
CODMAN QUAD-LOCK STERILIZATION CONTAINER SYSTEM
General Hospital
90d
Cleared
Mar 25, 2010
CODMAN STERILIZATION CONTAINERS
General Hospital
230d
Cleared
Jul 16, 1990
CODMAN SUCTION PATTIE
General Hospital
77d
Cleared
Jun 20, 1977
PRESERVE LUBRICANT CODE NO. 43=4035
General Hospital
98d