FDA 510(k) Applications Submitted by GEN-PROBE PRODESSE, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K132129 07/10/2013 PRODESSE PROFLU+ ASSAY GEN-PROBE PRODESSE, INC.
K132237 07/18/2013 PRODESSE PROFAST+ ASSAY GEN-PROBE PRODESSE, INC.
K132238 07/18/2013 PROPARAFLU+ ASSAY GEN-PROBE PRODESSE, INC.
K123274 10/19/2012 PROGASTRO SSCS ASSAY GEN-PROBE PRODESSE, INC.
K123838 12/13/2012 PRO HMPV+ ASSAY GEN-PROBE PRODESSE, INC.


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