FDA 510(k) Applications Submitted by LAKSHMI ANNE

FDA 510(k) Number Submission Date Device Name Applicant
K030649 02/28/2003 DRI COTININE EIA ASSAY MICROGENICS CORP.
K023617 10/29/2002 DRI METHADONE METABOLITE ENZYME IMMUNOASSAY MICROGENICS CORP.
K023780 11/12/2002 DRI PRIMIDONE CALIBRATORS MICROGENICS CORP.


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