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FDA 510(k) Applications Submitted by PRODESSE, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K081030
04/11/2008
MODIFICATION TO PROFLU+ ASSAY
PRODESSE, INC.
K091053
04/13/2009
PROPARAFLU+ASSAY
PRODESSE, INC.
K082688
09/15/2008
PRO HMPV+ ASSAY
PRODESSE, INC.
K073029
10/29/2007
PROFLU+ ASSAY
PRODESSE, INC.
K090239
02/02/2009
PROGASTRO CD ASSAY
PRODESSE, INC.
K092500
08/14/2009
MODIFICATION TO PROFLU+ ASSAY
PRODESSE, INC.
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