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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