Cordis Corp. - FDA 510(k) Cleared Devices
315
Total
281
Cleared
0
Denied
FDA 510(k) Regulatory Record - Cordis Corp. Neurology ✕
28 devices
Cleared
Dec 20, 1996
CORDIS SHARP-ENDED STYLET
Neurology
402d
Cleared
Oct 25, 1996
CORDIS STRAIGHT OR FINNED VENTR CATH (W/RADIO DOTS)
Neurology
288d
Cleared
Mar 25, 1996
CORDIS VENTRICULAR ANTECHAMBER (VA)
Neurology
90d
Cleared
Oct 19, 1995
CORDIS HORIZONTAL-VERICAL VALVE SYSTEM
Neurology
395d
Cleared
Mar 01, 1995
CORDIS DISPOSABLE ICP PRESSURE TRANSDUCER
Neurology
379d
Cleared
Jul 20, 1994
CORDIS GRAVITY COMPENSATING ACCESSORY
Neurology
426d
Cleared
Mar 02, 1994
CORDIS POLYPROPYLENE BURR HOLE RESERVOIR
Neurology
470d
Cleared
Aug 23, 1993
CORDIS TUNNELER
Neurology
102d
Cleared
Dec 10, 1992
INTEGRAL DRAINAGE/VENTRICULAR/LUMBAR DRAINAGE SETS
Neurology
90d
Cleared
Oct 30, 1992
CORDIS POLYPROPYLENE STRAIGHT, T & Y CONNECTOR
Neurology
189d
Cleared
Mar 09, 1992
CORDIS STRAIGHT VENTRICULAR CATHETER
Neurology
123d
Cleared
Feb 19, 1992
CORDIS RIGHT-ANGLE CATHETER GUIDE
Neurology
175d