FDA 510(k) Applications Submitted by KAREN HARRINGTON

FDA 510(k) Number Submission Date Device Name Applicant
K110968 04/06/2011 PROFLU+ ASSAY GEN-PROBE PRODESSE, INC
K081030 04/11/2008 MODIFICATION TO PROFLU+ ASSAY PRODESSE, INC.
K091053 04/13/2009 PROPARAFLU+ASSAY PRODESSE, INC.
K101855 07/01/2010 PROFAST+ ASSAY GEN-PROBE PRODESSE, INC
K082688 09/15/2008 PRO HMPV+ ASSAY PRODESSE, INC.
K123274 10/19/2012 PROGASTRO SSCS ASSAY GEN-PROBE PRODESSE, INC.
K073029 10/29/2007 PROFLU+ ASSAY PRODESSE, INC.
K123838 12/13/2012 PRO HMPV+ ASSAY GEN-PROBE PRODESSE, INC.


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