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FDA 510(k) Applications Submitted by PATHWORK DIAGNOSTICS, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K120489
02/17/2012
TISSUE OF ORIGIN TEST KIT FFPE
PATHWORK DIAGNOSTICS, INC.
K080896
03/31/2008
PATHWORK DIAGNOSTICS TISSUE OF ORIGIN TEST
PATHWORK DIAGNOSTICS, INC.
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