Cordis Corp. - FDA 510(k) Cleared Devices
315
Total
281
Cleared
0
Denied
FDA 510(k) Regulatory Record - Cordis Corp. General Hospital ✕
6 devices
Cleared
May 09, 1995
CORDIS CSF RESERVOIR
General Hospital
103d
Cleared
Mar 06, 1984
HYPODERMIC SYRINGES & NEEDLES
General Hospital
70d
Cleared
Jan 19, 1983
VARIOUS-SPECIMEN COLLECTORS
General Hospital
36d
Cleared
Aug 20, 1981
INTRAVENOUS ADMINISTRATION SET
General Hospital
9d
Cleared
Oct 23, 1980
CORDIS DOW INFUSION PUMP
General Hospital
31d
Cleared
Feb 01, 1979
MANIFOLD, DISPOSABLE 3 VALVE
General Hospital
30d