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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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