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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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