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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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