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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