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FDA 510(k) Applications Submitted by AGENDIA
FDA 510(k) Number
Submission Date
Device Name
Applicant
K081092
04/17/2008
MODIFICATION TO MAMMAPRINT
AGENDIA
K141142
05/02/2014
MAMMAPRINT FFPE
AGENDIA
K101454
05/25/2010
MAMMAPRINT
AGENDIA
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