Kenlor Industries, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kenlor Industries, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Kenlor Industries, Inc. has 9 FDA 510(k) cleared medical devices. Based in Westminster, US.
Historical record: 9 cleared submissions from 1989 to 1997. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Kenlor Industries, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kenlor Industries, Inc.
9 devices
Cleared
Mar 03, 1997
KENLOR H. PYLORI CONTROL SERUM
Microbiology
147d
Cleared
Jul 19, 1995
KENLOR LIQUID TOTAL URINE CONTROL
Chemistry
28d
Cleared
Mar 20, 1995
KENLOR HUMAN SPINAL FLUID CONTROL
Chemistry
61d
Cleared
Sep 07, 1990
KENLOR THERAPEUTIC DRUG MONITORING (TDM) CONTROL
Chemistry
44d
Cleared
Feb 16, 1990
KENLOR PYROGALLOL RED MICROPROTEIN ASSAY KIT
Chemistry
99d
Cleared
May 22, 1989
COOMASSIE BLUE TOTAL PROTEIN ASSAY KIT
Chemistry
104d
Cleared
Mar 24, 1989
KENLOR TOTAL IRON, UIBC/TIBC ASSAY KIT
Chemistry
46d
Cleared
Mar 09, 1989
KENLOR HUMAN SPINAL FLUID CONTROL LIQUID
Chemistry
31d
Cleared
Mar 09, 1989
KENLOR LIQUID URINE CONTROL
Chemistry
31d