FDA 510(k) Applications Submitted by PHOENIX BIOTECH CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K001552 05/18/2000 TREPCHEK TREPONEMAL ANTIBODY EIA PHOENIX BIOTECH CORP.
K053570 12/22/2005 TREP-SURE TREPONEMAL ANTIBODY EIA PHOENIX BIOTECH CORP.


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