FDA 510(k) Applications Submitted by CARDINAL HEALTH GERMANY 234 GMBH

FDA 510(k) Number Submission Date Device Name Applicant
K090486 02/25/2009 ASTHMA MONITOR MODEL, AM1 CARDINAL HEALTH GERMANY 234 GMBH
K082539 09/02/2008 MASTERSCOPE, MASTERSCOPE ECG, MASTERSCOPE CT CARDINAL HEALTH GERMANY 234 GMBH


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