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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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