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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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