Kenwell International , Ltd. is one of 87 FDA 510(k) medical device manufacturers from India in the dataset, ranked by real submission volume.
Kenwell International , Ltd. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Kenwell International , Ltd. has 5 FDA 510(k) cleared medical devices. Based in Karnataka, Karnataka, IN.
Historical record: 5 cleared submissions from 1990 to 1998. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Kenwell International , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kenwell International , Ltd.
5 devices
Cleared
Apr 08, 1998
COLOURED POWDWR-FREE SURGICAL GLOVES
General Hospital
64d
Cleared
Apr 03, 1998
STERILE POWDER-FREE LATEX EXAMINATION GLOVES
General Hospital
32d
Cleared
Nov 27, 1996
GLOVEL GX
General Hospital
114d
Cleared
Jul 12, 1991
SURGICAL GLOVES
General Hospital
120d
Cleared
Mar 09, 1990
LATEX PATIENT EXAMINATION GLOVES
General Hospital
16d