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FDA 510(k) Applications Submitted by CILAG GMBH INTERNATIONAL
FDA 510(k) Number
Submission Date
Device Name
Applicant
K110637
03/04/2011
ONETOUCH VERIO (TM) IQ BLOOD GLUCOSE MONITORING SYSTEM
CILAG GMBH INTERNATIONAL
K120708
03/08/2012
ONETOUCH VERIO SYNC BLOOD GLUCOSE MONITORING SYSTEM
CILAG GMBH INTERNATIONAL
K131363
05/13/2013
ONETOUCH VERIO BLOOD GLUCOSE MONITORING SYSTEM
CILAG GMBH INTERNATIONAL
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