FDA 510(k) Applications Submitted by BIOGENEX LABORATORIES

FDA 510(k) Number Submission Date Device Name Applicant
K012960 09/04/2001 BIOGENEX MONOCLONAL ANTI-PROGESTERONE RECEPTOR BIOGENEX LABORATORIES
K013148 09/20/2001 BIOGENEX MONOCLONAL ANTI-ESTROGEN RECEPTOR(CLONE ER88) BIOGENEX LABORATORIES


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