Medical Device Manufacturer · CH , Zug

Cilag GmbH International - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2011
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.

FDA 510(k) Regulatory Record - Cilag GmbH International

3 devices
1-3 of 3
Cleared Aug 30, 2013
ONETOUCH VERIO BLOOD GLUCOSE MONITORING SYSTEM
K131363 · NBW
Chemistry · 109d
Cleared Feb 07, 2013
ONETOUCH VERIO SYNC BLOOD GLUCOSE MONITORING SYSTEM
K120708 · NBW
Chemistry · 336d
Cleared Sep 07, 2011
ONETOUCH VERIO (TM) IQ BLOOD GLUCOSE MONITORING SYSTEM
K110637 · LFR
Chemistry · 187d
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