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FDA 510(k) Applications Submitted by RICK SPRING
FDA 510(k) Number
Submission Date
Device Name
Applicant
K090111
01/16/2009
FLEXPEN NEEDLE
NOVO NORDISK INC.
K062500
08/25/2006
FLEXPEN NEEDLE
NOVO NORDISK INC.
K133738
12/09/2013
NOVOFINE PLUS 32G 4 MM
NOVO NORDISK INC.
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