Ceragem Medisys, Inc. is one of 5120 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ceragem Medisys, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Ceragem Medisys, Inc. has 4 FDA 510(k) cleared medical devices. Based in Los Angeles, US.
Historical record: 4 cleared submissions from 2013 to 2014. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Ceragem Medisys, Inc. Filter by specialty or product code using the sidebar.
Ceragem Medisys, Inc. — FDA 510(k) Products and Clearance History
4 devices
Cleared
Sep 24, 2014
GLUCOVITAAL H1A BLOOD GLUCOSE MONITORING SYSTEM
Chemistry
79d
Cleared
Jul 03, 2014
LABONACHECK GLUPPY BLOOD GLUCOSE MONITORING SYSTEM
Chemistry
162d
Cleared
Feb 28, 2014
CERA-CHEK 1070 BLOOD GLUCOSE MONITORING SYSTEM
Chemistry
261d
Cleared
Feb 11, 2013
LABONACHECK GLUPPY BLOOD GLUCOSE MONITORING SYSTEM
Chemistry
872d