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FDA 510(k) Applications Submitted by MARIA CARMELITA S BALUYOT
FDA 510(k) Number
Submission Date
Device Name
Applicant
DEN110012
04/13/2011
APTIMA TRICHOMONAS VAGINALIS ASSAY
GEN-PROBE INCORPORATED
K122062
07/13/2012
APTIMA TRICHOMONAS VAGINALIS ASSAY - PANTHER
GEN-PROBE, INC.
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