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. Ophthalmic ✕
8 devices
Cleared
Dec 11, 1984
MICRA DIAMOND KNIFE MICRA ADJUSTABLE KNIFE
Ophthalmic
20d
Cleared
Oct 24, 1978
BAYLOW VISUAL ACUITY TESTER
Ophthalmic
62d
Cleared
Oct 11, 1978
OSCILLATING KNIFE AND ACCESSORIES
Ophthalmic
57d
Cleared
Sep 20, 1978
CORNEAL CUTTER AND ACCESSORIES
Ophthalmic
36d
Cleared
Sep 20, 1978
MICROSURGICAL KNIVES, 20, 30, 45
Ophthalmic
26d
Cleared
Mar 14, 1977
LENS SET, MENTOR TRIAL
Ophthalmic
14d
Cleared
Oct 15, 1976
SOLA COMMIDO LOUPE
Ophthalmic
11d
Cleared
Oct 15, 1976
SOLA SCHULTZE-CROCK OPTHALMOSCOPE
Ophthalmic
11d