Barriermed Glove Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Barriermed Glove Co. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Barriermed Glove Co. has 5 FDA 510(k) cleared medical devices. Based in Lake Mary, US.
Historical record: 5 cleared submissions from 1999 to 2006. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Barriermed Glove Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Barriermed Glove Co.
5 devices
Cleared
Jul 05, 2006
BARRIERPLUS GOLD POWDER-FREE SYNTHETIC POLYISOPRENE SURGICAL GLOVES
General Hospital
210d
Cleared
Jun 23, 2006
BARRIERPLUS PLATINUM POWDER-FREE SYNTHETIC POLYCHLOROPRENE SURGICAL GLOVES,...
General Hospital
70d
Cleared
Dec 20, 2005
BARRIERPLUS GOLD ORTHO POWDER-FREE SYNTHETIC POLYISOPRENE ORTHOPEDIC SURGICAL...
General Hospital
78d
Cleared
Nov 30, 2005
SYNTHALON PC PLUS POWDER-FREE POLYCHLOROPRENE EXAMINATION GLOVES, MODELS...
General Hospital
47d
Cleared
May 20, 1999
BARRIERPLUS SYNTHETIC POWDER-FREE SURGICAL GLOVES
General Hospital
77d