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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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