Codan Medlon, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Codan Medlon, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Codan Medlon, Inc. has 4 FDA 510(k) cleared medical devices. Based in Chester, US.
Historical record: 4 cleared submissions from 1996 to 1996. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Codan Medlon, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Codan Medlon, Inc.
4 devices
Cleared
Aug 20, 1996
POWDERFREE LATEX EXAM GLOVES WITH PROTEIN CONTENT LABELING CLAIM
General Hospital
371d
Cleared
Aug 20, 1996
BLUE LATEX EXAM GLOVES WITH PROTEIN CONTENT LABELING CLAIM
General Hospital
371d
Cleared
Aug 20, 1996
POWDERFREE BLUE LATEX EXAM GLOVES WITH PROTEIN CONTENT LABELING CLAIM
General Hospital
371d
Cleared
Apr 17, 1996
CODAN MEDLON BC110 VIAL ADAPTER CODAN SPIKE
General Hospital
42d