Kanam Latex Industries Pvt. , Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kanam Latex Industries Pvt. , Ltd. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Kanam Latex Industries Pvt. , Ltd. has 5 FDA 510(k) cleared medical devices. Based in Raphine, US.
Historical record: 5 cleared submissions from 1990 to 2005. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Kanam Latex Industries Pvt. , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kanam Latex Industries Pvt. , Ltd.
5 devices
Cleared
Sep 13, 2005
PRE-POWDERED STERILE EXAM GLOVES
General Hospital
29d
Cleared
Feb 24, 2004
POWDER FREE LATEX SURGEONS GLOVES POLYMER COATED STERILE WITH OPTIONAL...
General Hospital
104d
Cleared
Feb 06, 2002
POWDERFREE LATEX SURGEON'S GLOVES
General Hospital
71d
Cleared
Jan 31, 1991
SURGICARE STERILE SURGICAL GLOVES
General Hospital
99d
Cleared
Jan 23, 1990
LATEX PATIENT EXAMINATION GLOVES
General Hospital
27d