FDA 510(k) Applications Submitted by JOHN RIZOS

FDA 510(k) Number Submission Date Device Name Applicant
K120009 01/03/2012 TESTOSTERONE TEST SYSTEM; CALIBRATOR; AND QUALITY CONTROL MATERIAL (ASSAYED AND UNASSAYED) ABBOTT LABORATORIES
K111023 04/13/2011 ABBOTT ARCHITECT LH CALIBRATORS ABBOTT LABORATORIES


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