Winfield Co., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Winfield Co., Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Winfield Co., Inc. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1980 to 1994. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Winfield Co., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Winfield Co., Inc.
5 devices
Cleared
Dec 15, 1994
SHARPS-TAINER SMALL OPENING W/NEEDLE REMOVER
General Hospital
231d
Cleared
Sep 19, 1994
SHARPS-TAINER LARGE OPENING
General Hospital
144d
Cleared
Sep 19, 1994
SHARPS-TAINER SMALL OPENING
General Hospital
144d
Cleared
Jun 22, 1989
WINFIELD LATEX EXAMINATION GLOVES
General Hospital
87d
Cleared
Nov 19, 1980
CONVALESCENT RECLINER
Physical Medicine
16d