W.A. Rubbermate Co., Ltd. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
W.A. Rubbermate Co., Ltd. has 4 FDA 510(k) cleared medical devices. Based in Bristol, US.
Latest FDA clearance: Feb 2024. Active since 1997. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by W.A. Rubbermate Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - W.A. Rubbermate Co., Ltd.
4 devices
Cleared
Feb 13, 2024
Black Nitrile Powder Free Patient Examination Glove, Non Sterile
General Hospital
83d
Cleared
Jul 13, 2011
POWDER FREE NITRILE EXAMINATION GLOVES
General Hospital
149d
Cleared
Jul 30, 2002
WA RUBBERMATE LATEX POWDER-FREE EXAM GLOVES
General Hospital
120d
Cleared
Aug 29, 1997
W.A.
General Hospital
150d