Cilag GmbH International is one of 88 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Cilag GmbH International - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Cilag GmbH International has 3 FDA 510(k) cleared medical devices. Based in Zug, CH.
Historical record: 3 cleared submissions from 2011 to 2013. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Cilag GmbH International Filter by specialty or product code using the sidebar.
Cilag GmbH International — FDA 510(k) Products and Clearance History
3 devices
Cleared
Aug 30, 2013
ONETOUCH VERIO BLOOD GLUCOSE MONITORING SYSTEM
Chemistry
109d
Cleared
Feb 07, 2013
ONETOUCH VERIO SYNC BLOOD GLUCOSE MONITORING SYSTEM
Chemistry
336d
Cleared
Sep 07, 2011
ONETOUCH VERIO (TM) IQ BLOOD GLUCOSE MONITORING SYSTEM
Chemistry
187d