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FDA 510(k) Applications Submitted by MICROPHAGE, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K120563
02/24/2012
KEYPATH MRSA/MSSA BLOOD CULTURE TEST-BT
MICROPHAGE, INC.
K102342
08/18/2010
KEYPATH(TM) MRSA/MSSA BLOOD CULTURE TEST- BT
MICROPHAGE, INC.
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