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Phoenix Biotech Corp.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K053570
TREP-SURE TREPONEMAL ANTIBODY EIA
August 7, 2006
K001552
TREPCHEK TREPONEMAL ANTIBODY EIA
October 19, 2000