FDA 510(k) Applications Submitted by YD DIAGNOSTICS CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K060953 04/06/2006 OCCULTECH FECAL OCCULT BLOOD RAPID TEST YD DIAGNOSTICS CORP.
K141874 07/11/2014 URISCAN OPTIMA YD DIAGNOSTICS CORP.


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